Variant report

Variant	esv3441398
Chromosome Location	chr7:100170241-100172789
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:214)
CpG islands
(count:610)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:214 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr7:100171434-100171805	HepG2	liver:	n/a	n/a
2	BRCA1	chr7:100170930-100171090	HepG2	liver:	n/a	n/a
3	CCNT2	chr7:100171482-100171682	K562	blood:	n/a	n/a
4	CEBPD	chr7:100170894-100171141	HepG2	liver:	n/a	n/a
5	CHD2	chr7:100168579-100174037	HepG2	liver:	n/a	n/a
6	CREB1	chr7:100171385-100171718	A549	lung:	n/a	n/a
7	CTCF	chr7:100171517-100171591	NHEK	skin:	n/a	n/a
8	CTCF	chr7:100171480-100171630	HMEC	breast:	n/a	n/a
9	CTCF	chr7:100170220-100170370	BJ	skin:	n/a	n/a
10	CTCF	chr7:100171540-100171690	HEEpiC	esophagus:	n/a	n/a
11	CTCF	chr7:100171393-100171670	A549	lung:	n/a	n/a
12	CTCF	chr7:100171547-100171616	GM13977	blood:	n/a	n/a
13	CTCF	chr7:100170336-100170560	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr7:100171480-100171630	AG04449	skin:	n/a	n/a
15	CTCF	chr7:100171560-100171710	HA-sp	spinal cord:	n/a	n/a
16	CTCF	chr7:100171500-100171650	GM12878	blood:	n/a	n/a
17	CTCF	chr7:100171540-100171690	HEK293	kidney:	n/a	n/a
18	CTCF	chr7:100171503-100171629	HepG2	liver:	n/a	n/a
19	CTCF	chr7:100171490-100171621	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr7:100171368-100171718	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr7:100170360-100170510	Caco-2	colon:	n/a	n/a
22	CTCF	chr7:100171391-100171870	A549	lung:	n/a	n/a
23	CTCF	chr7:100171500-100171650	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr7:100171460-100171610	A549	lung:	n/a	n/a
25	CTCF	chr7:100171540-100171690	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr7:100171460-100171610	HA-sp	spinal cord:	n/a	n/a
27	CTCF	chr7:100170340-100170490	HepG2	liver:	n/a	n/a
28	CTCF	chr7:100171442-100171679	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr7:100170320-100170470	GM06990	blood:	n/a	n/a
30	CTCF	chr7:100170440-100170590	GM06990	blood:	n/a	n/a
31	CTCF	chr7:100171540-100171690	GM12871	blood:	n/a	n/a
32	CTCF	chr7:100171500-100171650	BJ	skin:	n/a	n/a
33	CTCF	chr7:100170440-100170590	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr7:100170420-100170519	GM12891	blood:	n/a	n/a
35	CTCF	chr7:100171500-100171650	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr7:100171400-100171550	HVMF	connective:	n/a	n/a
37	CTCF	chr7:100171460-100171640	A549	lung:	n/a	n/a
38	CTCF	chr7:100171559-100171564	GM10248	blood:	n/a	n/a
39	CTCF	chr7:100171480-100171630	SAEC	small airway:	n/a	n/a
40	CTCF	chr7:100171500-100171650	HPF	lung:	n/a	n/a
41	CTCF	chr7:100171513-100171516	GM19238	blood:	n/a	n/a
42	CTCF	chr7:100171540-100171690	AG09319	gingival:	n/a	n/a
43	CTCF	chr7:100171419-100171677	HepG2	liver:	n/a	n/a
44	CTCF	chr7:100171568-100171593	GM10248	blood:	n/a	n/a
45	CTCF	chr7:100171518-100171531	GM13977	blood:	n/a	n/a
46	CTCF	chr7:100171295-100171741	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr7:100171539-100171602	LNCaP	prostate:	n/a	n/a
48	CTCF	chr7:100171520-100171670	NHEK	skin:	n/a	n/a
49	CTCF	chr7:100170420-100170570	HepG2	liver:	n/a	n/a
50	CTCF	chr7:100170399-100170508	H1-hESC	embryonic stem cell:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:100171617-100171667	GM12892	blood:	n/a
2	chr7:100170610-100170660	HRE	kidney:	n/a
3	chr7:100171158-100171208	K562	blood:	n/a
4	chr7:100170496-100170546	IMR90	lung:	fetal
5	chr7:100171158-100171208	MCF10A-Er-Src	breast:	n/a
6	chr7:100171198-100171248	MCF-7	breast:	n/a
7	chr7:100172231-100172281	Caco-2	colon:	n/a
8	chr7:100171932-100171982	AoSMC	blood vessel:	n/a
9	chr7:100170610-100170660	GM06990	blood:	n/a
10	chr7:100171198-100171248	LNCaP	prostate:	n/a
11	chr7:100170795-100170845	GM12891	blood:	n/a
12	chr7:100171158-100171208	HCT-116	colon:	n/a
13	chr7:100171617-100171667	GM06990	blood:	n/a
14	chr7:100171158-100171208	HEEpiC	esophagus:	n/a
15	chr7:100170610-100170660	NB4	blood:	n/a
16	chr7:100171748-100171798	H1-hESC	embryonic stem cell:	embryo
17	chr7:100170610-100170660	T-47D	breast:	n/a
18	chr7:100171748-100171798	GM12891	blood:	n/a
19	chr7:100170795-100170845	U87	brain:	n/a
20	chr7:100171748-100171798	AG04450	lung:	fetal
21	chr7:100170496-100170546	HL-60	blood:	n/a
22	chr7:100171198-100171248	NHBE	bronchial:	n/a
23	chr7:100172231-100172281	AG04449	skin:	fetal
24	chr7:100171932-100171982	HEEpiC	esophagus:	n/a
25	chr7:100171748-100171798	SK-N-SH	brain:	n/a
26	chr7:100170795-100170845	HRPEpiC	eye:	n/a
27	chr7:100171617-100171667	AG09319	gingival:	n/a
28	chr7:100170610-100170660	HEEpiC	esophagus:	n/a
29	chr7:100170610-100170660	ovcar-3	ovarian:	n/a
30	chr7:100171158-100171208	Caco-2	colon:	n/a
31	chr7:100170496-100170546	GM12892	blood:	n/a
32	chr7:100171158-100171208	LNCaP	prostate:	n/a
33	chr7:100170610-100170660	HepG2	liver:	n/a
34	chr7:100171198-100171248	NB4	blood:	n/a
35	chr7:100171158-100171208	SK-N-SH	brain:	n/a
36	chr7:100170610-100170660	NHDF-neo	bronchial:	n/a
37	chr7:100172231-100172281	HepG2	liver:	n/a
38	chr7:100170496-100170546	BJ	skin:	n/a
39	chr7:100170610-100170660	SK-N-MC	brain:	n/a
40	chr7:100170929-100170979	PrEC	prostate:	n/a
41	chr7:100170496-100170546	H1-hESC	embryonic stem cell:	embryo
42	chr7:100172231-100172281	NB4	blood:	n/a
43	chr7:100170929-100170979	T-47D	breast:	n/a
44	chr7:100170929-100170979	HUVEC	blood vessel:	n/a
45	chr7:100171748-100171798	HL-60	blood:	n/a
46	chr7:100172231-100172281	HIPEpiC	eye:	n/a
47	chr7:100170610-100170660	HNPCEpiC	eye:	n/a
48	chr7:100171158-100171208	HIPEpiC	eye:	n/a
49	chr7:100170610-100170660	Hepatocyte	liver:	n/a
50	chr7:100171158-100171208	Hepatocyte	liver:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:100033704..100035599-chr7:100167839..100170550,2	K562	blood:
2	chr7:100169248..100171474-chr7:100281930..100284276,2	MCF-7	breast:
3	chr7:100156035..100158297-chr7:100168691..100170406,2	MCF-7	breast:
4	chr7:100027524..100029226-chr7:100168230..100171158,2	K562	blood:
5	chr7:100142903..100145091-chr7:100168075..100170895,2	MCF-7	breast:
6	chr7:100167688..100170595-chr7:100808818..100810322,2	K562	blood:
7	chr7:100171397..100173664-chr7:100281141..100284646,3	K562	blood:

No data

Variant related genes	Relation type
SAP25	TF binding region
SAP25	CpG island
ENSG00000160813	chromatin interactions
ENSG00000240211	chromatin interactions
ENSG00000128564	chromatin interactions
ENSG00000146830	chromatin interactions

Extended variants
information (count: 115 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:115 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371699088	chr7:100170254-100170255	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs546546962	chr7:100170320-100170321	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs567978171	chr7:100170331-100170332	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs375203122	chr7:100170337-100170338	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs556504446	chr7:100170338-100170339	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs373789214	chr7:100170367-100170368	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs184836154	chr7:100170401-100170402	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs569254035	chr7:100170407-100170408	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs575400337	chr7:100170457-100170458	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs539633553	chr7:100170464-100170465	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs138765930	chr7:100170497-100170498	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs116230060	chr7:100170498-100170499	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs376397579	chr7:100170583-100170584	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs199499379	chr7:100170596-100170597	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs575059837	chr7:100170610-100170611	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs371163842	chr7:100170611-100170612	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs573938422	chr7:100170642-100170643	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs201295622	chr7:100170647-100170648	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs542184485	chr7:100170656-100170657	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs188928344	chr7:100170662-100170663	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs369560488	chr7:100170676-100170677	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs530868920	chr7:100170687-100170688	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs545972782	chr7:100170735-100170736	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs564294649	chr7:100170736-100170737	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs371316607	chr7:100170740-100170741	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs376583578	chr7:100170775-100170776	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs528153790	chr7:100170776-100170777	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs192702476	chr7:100170795-100170796	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs568173547	chr7:100170802-100170803	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs374270717	chr7:100170846-100170847	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs184117891	chr7:100170847-100170848	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs539485810	chr7:100170851-100170852	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs73156207	chr7:100170912-100170913	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs557904835	chr7:100171014-100171015	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs566741441	chr7:100171071-100171072	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs141701630	chr7:100171073-100171074	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs555558021	chr7:100171088-100171089	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs574124980	chr7:100171109-100171110	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs544271420	chr7:100171112-100171113	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs556607816	chr7:100171145-100171146	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs575579836	chr7:100171149-100171150	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs2686812	chr7:100171167-100171168	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs2686811	chr7:100171186-100171187	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs61052598	chr7:100171198-100171199	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs564405815	chr7:100171231-100171232	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs572930057	chr7:100171265-100171266	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs540465104	chr7:100171333-100171334	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs561616488	chr7:100171347-100171348	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs528990776	chr7:100171377-100171378	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs148046169	chr7:100171444-100171445	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Stenocardia	21860640	CNVD
Vasospasm	21860640	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
Acute lymphoblastic leukemia	21339820	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
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	21865298	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:214 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100154600-100173600	Weak transcription	HSMMtube	muscle
2	chr7:100160800-100172800	Weak transcription	Aorta	Aorta
3	chr7:100167000-100171800	Weak transcription	Small Intestine	intestine
4	chr7:100167600-100171200	Enhancers	Placenta Amnion	Placenta Amnion
5	chr7:100167600-100173600	Weak transcription	HSMM	muscle
6	chr7:100168000-100170600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:100168000-100171600	Weak transcription	Brain Substantia Nigra	brain
8	chr7:100168000-100172800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr7:100168000-100172800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr7:100168000-100179800	Weak transcription	Right Atrium	heart
11	chr7:100168200-100170400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr7:100168200-100170400	Enhancers	NH-A	brain
13	chr7:100168200-100170600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr7:100168200-100170600	Weak transcription	Colonic Mucosa	Colon
15	chr7:100168200-100170800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr7:100168200-100170800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
17	chr7:100168200-100170800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
18	chr7:100168200-100171600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr7:100168200-100171600	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr7:100168200-100172000	Weak transcription	Brain Anterior Caudate	brain
21	chr7:100168200-100172200	Weak transcription	Brain Hippocampus Middle	brain
22	chr7:100168200-100172600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr7:100168200-100172600	Weak transcription	Ovary	ovary
24	chr7:100168200-100172800	Weak transcription	Brain Angular Gyrus	brain
25	chr7:100168200-100172800	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr7:100168200-100177600	Weak transcription	HMEC	breast
27	chr7:100168400-100171000	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr7:100168400-100171200	Enhancers	H1 Cell Line	embryonic stem cell
29	chr7:100168600-100170800	Flanking Active TSS	HepG2	liver
30	chr7:100168600-100175200	Weak transcription	Osteobl	bone
31	chr7:100168600-100179600	Strong transcription	NHLF	lung
32	chr7:100168800-100170400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr7:100168800-100171000	Weak transcription	Adipose Nuclei	Adipose
34	chr7:100168800-100171600	Weak transcription	Stomach Smooth Muscle	stomach
35	chr7:100168800-100173800	Weak transcription	Primary hematopoietic stem cells	blood
36	chr7:100168800-100175400	Weak transcription	HUVEC	blood vessel
37	chr7:100168800-100175800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr7:100168800-100177400	Weak transcription	NHDF-Ad	bronchial
39	chr7:100169000-100170400	Weak transcription	Esophagus	oesophagus
40	chr7:100169000-100170600	Genic enhancers	Fetal Thymus	thymus
41	chr7:100169000-100171400	Weak transcription	Right Ventricle	heart
42	chr7:100169000-100171600	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr7:100169000-100171800	Weak transcription	Left Ventricle	heart
44	chr7:100169200-100170400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr7:100169200-100170400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr7:100169200-100170600	Weak transcription	Dnd41	blood
47	chr7:100169200-100170800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr7:100169200-100170800	Weak transcription	Gastric	stomach
49	chr7:100169200-100171600	Strong transcription	Spleen	Spleen
50	chr7:100169200-100172400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

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