Variant report

Variant	esv3439262
Chromosome Location	chr7:102107397-102110095
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102107670-102107707	HepG2	liver:	n/a	n/a
2	BRCA1	chr7:102107676-102107680	HepG2	liver:	n/a	n/a
3	BRCA1	chr7:102107666-102107866	Hela-S3	cervix:	n/a	n/a
4	CCNT2	chr7:102109140-102109266	K562	blood:	n/a	n/a
5	CHD2	chr7:102107547-102107747	GM12878	blood:	n/a	n/a
6	CTCF	chr7:102107660-102107810	HA-sp	spinal cord:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
7	CTCF	chr7:102107660-102107810	GM12870	blood:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
8	CTCF	chr7:102107559-102107801	MCF-7	breast:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
9	CTCF	chr7:102107609-102107767	GM10266	blood:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
10	CTCF	chr7:102107380-102107530	GM12868	blood:	n/a	n/a
11	CTCF	chr7:102107680-102107830	GM12864	blood:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
12	CTCF	chr7:102107640-102107790	GM12868	blood:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
13	CTCF	chr7:102107640-102107790	HepG2	liver:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
14	CTCF	chr7:102107620-102107770	MCF-7	breast:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
15	CTCF	chr7:102107545-102107814	ProgFib	skin:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
16	CTCF	chr7:102107620-102107770	Caco-2	colon:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
17	CTCF	chr7:102107589-102107825	SK-N-SH_RA	brain:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
18	CTCF	chr7:102107960-102108110	AG04449	skin:	n/a	n/a
19	CTCF	chr7:102107360-102107510	HL-60	blood:	n/a	n/a
20	CTCF	chr7:102107564-102107808	Gliobla	brain:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
21	CTCF	chr7:102107491-102107882	GM12878	blood:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
22	CTCF	chr7:102107585-102107813	HepG2	liver:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
23	CTCF	chr7:102107680-102107830	GM12873	blood:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
24	CTCF	chr7:102107600-102107750	HRPEpiC	eye:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
25	CTCF	chr7:102107640-102107790	HFF-Myc	foreskin:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
26	CTCF	chr7:102107680-102107830	GM12869	blood:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
27	CTCF	chr7:102107660-102107810	WI-38	lung:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
28	CTCF	chr7:102107680-102107830	HMF	breast:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
29	CTCF	chr7:102107516-102107792	GM12878	blood:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
30	CTCF	chr7:102107582-102107761	HUVEC	blood vessel:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
31	CTCF	chr7:102107620-102107770	NHDF-neo	bronchial:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
32	CTCF	chr7:102107380-102107530	GM12873	blood:	n/a	n/a
33	CTCF	chr7:102107483-102107857	A549	lung:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
34	CTCF	chr7:102107640-102107790	MCF-7	breast:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
35	CTCF	chr7:102109280-102109430	BE2_C	brain:	n/a	n/a
36	CTCF	chr7:102107620-102107770	GM12878	blood:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
37	CTCF	chr7:102107640-102107790	GM12864	blood:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
38	CTCF	chr7:102107768-102107770	GM10266	blood:	n/a	n/a
39	CTCF	chr7:102107660-102107810	AG09319	gingival:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
40	CTCF	chr7:102107660-102107810	GM12878	blood:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
41	CTCF	chr7:102107620-102107770	HCPEpiC	choroid plexus:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
42	CTCF	chr7:102107640-102107790	GM12873	blood:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
43	CTCF	chr7:102107589-102107753	GM20000	blood:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
44	CTCF	chr7:102107595-102107754	A549	lung:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
45	CTCF	chr7:102107360-102107510	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr7:102107540-102107544	ProgFib	skin:	n/a	n/a
47	CTCF	chr7:102107901-102108009	GM19238	blood:	n/a	n/a
48	CTCF	chr7:102107620-102107770	HUVEC	blood vessel:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
49	CTCF	chr7:102107557-102107790	T-47D	breast:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
50	CTCF	chr7:102107469-102107829	GM12892	blood:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102107737-102107787	SK-N-SH	brain:	n/a
2	chr7:102107737-102107787	GM06990	blood:	n/a
3	chr7:102109095-102109145	HCF	heart:	n/a
4	chr7:102107737-102107787	HRPEpiC	eye:	n/a
5	chr7:102109247-102109297	HRPEpiC	eye:	n/a
6	chr7:102109446-102109496	NHDF-neo	bronchial:	n/a
7	chr7:102109247-102109297	HIPEpiC	eye:	n/a
8	chr7:102109446-102109496	Jurkat	blood:	n/a
9	chr7:102109446-102109496	HMEC	breast:	n/a
10	chr7:102107737-102107787	HRCEpiC	kidney:	n/a
11	chr7:102107737-102107787	SAEC	small airway:	n/a
12	chr7:102109095-102109145	CMK	blood:	n/a
13	chr7:102109095-102109145	MCF-7	breast:	n/a
14	chr7:102107737-102107787	AG04449	skin:	fetal
15	chr7:102109247-102109297	AG09319	gingival:	n/a
16	chr7:102109247-102109297	SAEC	small airway:	n/a
17	chr7:102109247-102109297	ovcar-3	ovarian:	n/a
18	chr7:102107737-102107787	NB4	blood:	n/a
19	chr7:102107737-102107787	GM19239	blood:	n/a
20	chr7:102107737-102107787	H1-hESC	embryonic stem cell:	embryo
21	chr7:102107737-102107787	HCF	heart:	n/a
22	chr7:102109446-102109496	HCT-116	colon:	n/a
23	chr7:102109446-102109496	HCF	heart:	n/a
24	chr7:102107737-102107787	RPTEC	kidney:	n/a
25	chr7:102109095-102109145	AG09309	skin:	n/a
26	chr7:102109446-102109496	HL-60	blood:	n/a
27	chr7:102109095-102109145	HCM	heart:	n/a
28	chr7:102107737-102107787	AG10803	skin:	n/a
29	chr7:102107737-102107787	HMEC	breast:	n/a
30	chr7:102109247-102109297	MCF10A-Er-Src	breast:	n/a
31	chr7:102107737-102107787	PrEC	prostate:	n/a
32	chr7:102109095-102109145	T-47D	breast:	n/a
33	chr7:102109095-102109145	SK-N-SH_RA	brain:	n/a
34	chr7:102109446-102109496	GM12878	blood:	n/a
35	chr7:102109095-102109145	PFSK-1	brain:	n/a
36	chr7:102109446-102109496	ProgFib	skin:	n/a
37	chr7:102107737-102107787	BJ	skin:	n/a
38	chr7:102109095-102109145	MCF10A-Er-Src	breast:	n/a
39	chr7:102109247-102109297	HEEpiC	esophagus:	n/a
40	chr7:102109446-102109496	HPAEpiC	pulmonary alveolar:	n/a
41	chr7:102107737-102107787	AG04450	lung:	fetal
42	chr7:102109247-102109297	PrEC	prostate:	n/a
43	chr7:102107737-102107787	HCM	heart:	n/a
44	chr7:102109095-102109145	A549	lung:	n/a
45	chr7:102109446-102109496	SKMC	muscle:	n/a
46	chr7:102109247-102109297	T-47D	breast:	n/a
47	chr7:102109095-102109145	HUVEC	blood vessel:	n/a
48	chr7:102109247-102109297	GM19239	blood:	n/a
49	chr7:102109095-102109145	AG09319	gingival:	n/a
50	chr7:102109446-102109496	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:102074336..102076927-chr7:102105688..102108273,2	K562	blood:
2	chr7:101929851..101931493-chr7:102106221..102107741,2	MCF-7	breast:

Variant related genes	Relation type
ALKBH4	TF binding region
MIR4467	TF binding region
LRWD1	TF binding region
ALKBH4	CpG island
MIR4467	CpG island
LRWD1	CpG island
ENSG00000160991	chromatin interactions
ENSG00000239480	chromatin interactions

Extended variants
information (count: 189 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:189 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554235428	chr7:102107430-102107431	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs142846955	chr7:102107451-102107452	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs536366930	chr7:102107468-102107469	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs554611259	chr7:102107508-102107509	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs374197328	chr7:102107517-102107518	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs200404259	chr7:102107518-102107519	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs59522694	chr7:102107536-102107537	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs374774982	chr7:102107565-102107566	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs67404811	chr7:102107566-102107567	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs112957064	chr7:102107573-102107574	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs111263407	chr7:102107574-102107575	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs60020010	chr7:102107585-102107586	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs565268696	chr7:102107587-102107588	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs147361915	chr7:102107608-102107609	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs11764925	chr7:102107615-102107616	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs13225204	chr7:102107618-102107619	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs13225212	chr7:102107627-102107628	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs112938997	chr7:102107629-102107630	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs138754213	chr7:102107655-102107656	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs59898461	chr7:102107662-102107663	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs11761361	chr7:102107697-102107698	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs375287478	chr7:102107703-102107704	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs199763079	chr7:102107737-102107738	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs182170193	chr7:102107741-102107742	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs116645570	chr7:102107750-102107751	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs565966526	chr7:102107757-102107758	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs369279613	chr7:102107758-102107759	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs373355050	chr7:102107759-102107760	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs376398065	chr7:102107780-102107781	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs200451942	chr7:102107782-102107783	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs199699460	chr7:102107785-102107786	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs77359539	chr7:102107811-102107812	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs542708497	chr7:102107814-102107815	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs372583053	chr7:102107816-102107817	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs202069180	chr7:102107817-102107818	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs143788158	chr7:102107819-102107820	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs117163893	chr7:102107848-102107849	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs141905334	chr7:102107850-102107851	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs375573347	chr7:102107853-102107854	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs376444470	chr7:102107854-102107855	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs570334710	chr7:102107885-102107886	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs200102694	chr7:102107890-102107891	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs374442932	chr7:102107896-102107897	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs11538920	chr7:102107901-102107902	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs560973225	chr7:102107908-102107909	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs201978340	chr7:102107926-102107927	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs201107348	chr7:102107942-102107943	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs371118705	chr7:102107943-102107944	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs187183988	chr7:102107973-102107974	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs569864916	chr7:102107996-102107997	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:265 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102106000-102107800	Enhancers	Fetal Brain Male	brain
2	chr7:102106000-102107800	Enhancers	Spleen	Spleen
3	chr7:102106000-102108000	Enhancers	Fetal Heart	heart
4	chr7:102106400-102107400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr7:102106400-102107600	Enhancers	Primary B cells from cord blood	blood
6	chr7:102106400-102107600	Genic enhancers	Primary B cells from peripheral blood	blood
7	chr7:102106400-102108000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr7:102106400-102108000	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr7:102106400-102108400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr7:102106400-102110000	Enhancers	Liver	Liver
11	chr7:102106400-102111000	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr7:102106400-102112600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr7:102106400-102112600	Weak transcription	Aorta	Aorta
14	chr7:102106400-102119400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr7:102106600-102107400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr7:102106600-102107400	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr7:102106600-102107800	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr7:102106600-102107800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
19	chr7:102106600-102107800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr7:102106600-102107800	Enhancers	Fetal Thymus	thymus
21	chr7:102106600-102108000	Genic enhancers	Fetal Intestine Small	intestine
22	chr7:102106600-102108000	Weak transcription	Thymus	Thymus
23	chr7:102106600-102108200	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr7:102106600-102108200	Weak transcription	A549	lung
25	chr7:102106600-102108400	Weak transcription	Placenta	Placenta
26	chr7:102106600-102108600	Weak transcription	Osteobl	bone
27	chr7:102106600-102108800	Genic enhancers	Primary T cells fromperipheralblood	blood
28	chr7:102106600-102110000	Weak transcription	Stomach Mucosa	stomach
29	chr7:102106600-102110200	Weak transcription	Small Intestine	intestine
30	chr7:102106600-102112400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr7:102106600-102112600	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr7:102106600-102112600	Weak transcription	Ovary	ovary
33	chr7:102106600-102112800	Weak transcription	Psoas Muscle	Psoas
34	chr7:102106600-102112800	Weak transcription	HSMMtube	muscle
35	chr7:102106600-102112800	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr7:102106600-102113200	Weak transcription	Fetal Lung	lung
37	chr7:102106600-102115000	Weak transcription	Primary hematopoietic stem cells	blood
38	chr7:102106600-102119200	Weak transcription	Right Atrium	heart
39	chr7:102106800-102107400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr7:102106800-102107400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr7:102106800-102107400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr7:102106800-102107400	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr7:102106800-102107400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
44	chr7:102106800-102107400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr7:102106800-102107400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr7:102106800-102107400	Weak transcription	Fetal Muscle Leg	muscle
47	chr7:102106800-102107400	Weak transcription	Lung	lung
48	chr7:102106800-102107400	Genic enhancers	Stomach Smooth Muscle	stomach
49	chr7:102106800-102107600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr7:102106800-102107600	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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