Variant report

Variant	nsv511361
Chromosome Location	chr7:100548960-100553306
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:292)
CpG islands
(count:62)
Chromatin interactive
region (count:8)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:100550350-100551274	K562	blood:	n/a	n/a
2	ATF2	chr7:100548745-100549225	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:100548761-100549286	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:100548883-100549254	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:100550402-100551274	K562	blood:	n/a	n/a
6	BCL3	chr7:100550248-100551440	A549	lung:	n/a	n/a
7	BHLHE40	chr7:100550634-100551200	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:100550595-100551382	K562	blood:	n/a	n/a
9	BRCA1	chr7:100550597-100551380	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr7:100550522-100551358	GM12878	blood:	n/a	n/a
11	BRCA1	chr7:100550256-100551378	HepG2	liver:	n/a	n/a
12	CBX3	chr7:100550582-100551391	K562	blood:	n/a	n/a
13	CEBPB	chr7:100548882-100549443	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr7:100549547-100549857	HepG2	liver:	n/a	chr7:100549687-100549698
15	CEBPB	chr7:100549541-100549829	A549	lung:	n/a	chr7:100549687-100549698
16	CEBPB	chr7:100549521-100549841	K562	blood:	n/a	chr7:100549687-100549698
17	CEBPZ	chr7:100550215-100551674	HepG2	liver:	n/a	n/a
18	CHD1	chr7:100550597-100551381	GM12878	blood:	n/a	n/a
19	CHD2	chr7:100548864-100549412	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr7:100550632-100551367	K562	blood:	n/a	n/a
21	CHD2	chr7:100550522-100551352	HepG2	liver:	n/a	n/a
22	CHD2	chr7:100550607-100551235	GM12878	blood:	n/a	n/a
23	CHD2	chr7:100550634-100551218	Hela-S3	cervix:	n/a	n/a
24	CTBP2	chr7:100548802-100549986	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr7:100550680-100550830	GM12865	blood:	n/a	n/a
26	CTCF	chr7:100548932-100549007	LNCaP	prostate:	n/a	n/a
27	CTCF	chr7:100550700-100550850	GM12867	blood:	n/a	n/a
28	CTCF	chr7:100551800-100551950	GM12864	blood:	n/a	n/a
29	CTCF	chr7:100550680-100550830	GM12872	blood:	n/a	n/a
30	CTCF	chr7:100550680-100550830	HMF	breast:	n/a	n/a
31	CTCF	chr7:100550680-100550830	AG09319	gingival:	n/a	n/a
32	CTCF	chr7:100551020-100551170	GM12878	blood:	n/a	n/a
33	CTCF	chr7:100550880-100551030	MCF-7	breast:	n/a	n/a
34	CTCF	chr7:100550680-100550830	AG04450	lung:	n/a	n/a
35	CTCF	chr7:100550680-100550830	GM12864	blood:	n/a	n/a
36	CTCF	chr7:100550700-100550850	GM12868	blood:	n/a	n/a
37	CTCF	chr7:100550680-100550830	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr7:100550720-100550870	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr7:100550820-100551050	AG09309	skin:	n/a	n/a
40	CTCF	chr7:100550960-100551110	AG04450	lung:	n/a	n/a
41	CTCF	chr7:100550720-100550870	GM12864	blood:	n/a	n/a
42	CTCF	chr7:100549560-100549710	Caco-2	colon:	n/a	n/a
43	CTCF	chr7:100550720-100550870	BE2_C	brain:	n/a	n/a
44	CTCF	chr7:100549575-100549625	MCF-7	breast:	n/a	n/a
45	CTCF	chr7:100551980-100552130	GM12872	blood:	n/a	n/a
46	CTCF	chr7:100550680-100550830	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr7:100550774-100550861	LNCaP	prostate:	n/a	n/a
48	CTCF	chr7:100550700-100550850	RPTEC	kidney:	n/a	n/a
49	CTCF	chr7:100551040-100551190	AG04450	lung:	n/a	n/a
50	CTCF	chr7:100550720-100550870	HFF	foreskin:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:100550138-100550188	HNPCEpiC	eye:	n/a
2	chr7:100550138-100550188	HNPCEpiC	eye:	n/a
3	chr7:100550138-100550188	HEEpiC	esophagus:	n/a
4	chr7:100550138-100550188	NT2-D1	testis:	n/a
5	chr7:100550138-100550188	HPAEpiC	pulmonary alveolar:	n/a
6	chr7:100550138-100550188	HEK293	kidney:	embryo
7	chr7:100550138-100550188	HIPEpiC	eye:	n/a
8	chr7:100550138-100550188	K562	blood:	n/a
9	chr7:100550138-100550188	SK-N-MC	brain:	n/a
10	chr7:100550138-100550188	IMR90	lung:	fetal
11	chr7:100550138-100550188	HMEC	breast:	n/a
12	chr7:100550138-100550188	AG04449	skin:	fetal
13	chr7:100550138-100550188	T-47D	breast:	n/a
14	chr7:100550138-100550188	HRPEpiC	eye:	n/a
15	chr7:100550138-100550188	ProgFib	skin:	n/a
16	chr7:100550138-100550188	Caco-2	colon:	n/a
17	chr7:100550138-100550188	AG10803	skin:	n/a
18	chr7:100550138-100550188	H1-hESC	embryonic stem cell:	embryo
19	chr7:100550138-100550188	NHDF-neo	bronchial:	n/a
20	chr7:100550138-100550188	MCF-7	breast:	n/a
21	chr7:100550138-100550188	AoSMC	blood vessel:	n/a
22	chr7:100550138-100550188	GM12892	blood:	n/a
23	chr7:100550138-100550188	GM19239	blood:	n/a
24	chr7:100550138-100550188	RPTEC	kidney:	n/a
25	chr7:100550138-100550188	HCT-116	colon:	n/a
26	chr7:100550138-100550188	HCPEpiC	choroid plexus:	n/a
27	chr7:100550138-100550188	BE2_C	brain:	n/a
28	chr7:100550138-100550188	HepG2	liver:	n/a
29	chr7:100550138-100550188	AG09309	skin:	n/a
30	chr7:100550138-100550188	PrEC	prostate:	n/a
31	chr7:100550138-100550188	PANC-1	pancreas:	n/a
32	chr7:100550138-100550188	U87	brain:	n/a
33	chr7:100550138-100550188	Hela-S3	cervix:	n/a
34	chr7:100550138-100550188	HL-60	blood:	n/a
35	chr7:100550138-100550188	SK-N-SH_RA	brain:	n/a
36	chr7:100550138-100550188	NH-A	brain:	n/a
37	chr7:100550138-100550188	ovcar-3	ovarian:	n/a
38	chr7:100550138-100550188	LNCaP	prostate:	n/a
39	chr7:100550138-100550188	SK-N-SH	brain:	n/a
40	chr7:100550138-100550188	BJ	skin:	n/a
41	chr7:100550138-100550188	HRE	kidney:	n/a
42	chr7:100550138-100550188	SAEC	small airway:	n/a
43	chr7:100550138-100550188	A549	lung:	n/a
44	chr7:100550138-100550188	GM12891	blood:	n/a
45	chr7:100550138-100550188	SKMC	muscle:	n/a
46	chr7:100550138-100550188	HUVEC	blood vessel:	n/a
47	chr7:100550138-100550188	Hepatocyte	liver:	n/a
48	chr7:100550138-100550188	CMK	blood:	n/a
49	chr7:100550138-100550188	HCF	heart:	n/a
50	chr7:100550138-100550188	ECC-1	luminal epithelium:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:100547706..100549637-chr7:100613917..100615692,2	MCF-7	breast:
2	chr7:100551774..100553775-chr7:100606595..100608318,2	MCF-7	breast:
3	chr7:100490569..100492448-chr7:100550621..100553306,2	MCF-7	breast:
4	chr7:100549832..100554872-chr7:100605467..100612701,10	K562	blood:
5	chr7:100549832..100555944-chr7:100607722..100611748,10	K562	blood:
6	chr7:100549275..100549788-chr7:100702024..100702894,2	MCF-7	breast:
7	chr7:100494043..100496246-chr7:100550371..100552219,2	K562	blood:
8	chr7:100493649..100495175-chr7:100549463..100550982,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACHE-5	chr7:100550661-100550705	NONHSAT122427
2	lnc-ACHE-5	chr7:100550808-100550858	NONHSAT122427
3	lnc-ACHE-5	chr7:100551165-100551637	NONHSAT122427
4	lnc-ACHE-4	chr7:100549481-100550424	NONHSAT122426

No data

Variant related genes	Relation type
MUC3A	TF binding region
MUC3A	CpG island
ENSG00000225946	chromatin interactions
ENSG00000169894	chromatin interactions
ENSG00000087085	chromatin interactions

Extended variants
information (count: 619 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:619 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530703940	chr7:100548975-100548976	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs545686117	chr7:100548989-100548990	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs117032923	chr7:100548991-100548992	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs76783748	chr7:100549012-100549013	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs145950291	chr7:100549022-100549023	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs548543369	chr7:100549024-100549025	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs552874186	chr7:100549037-100549038	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs546639202	chr7:100549041-100549042	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs79986815	chr7:100549047-100549048	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs80179794	chr7:100549048-100549049	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs78394277	chr7:100549050-100549051	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs76387827	chr7:100549052-100549053	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs75323441	chr7:100549055-100549056	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs76829389	chr7:100549064-100549065	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs528924712	chr7:100549083-100549084	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs368126177	chr7:100549085-100549086	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs75258237	chr7:100549092-100549093	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs80144465	chr7:100549098-100549099	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs569581414	chr7:100549100-100549101	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs201239284	chr7:100549105-100549106	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs36159280	chr7:100549106-100549107	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs540094011	chr7:100549107-100549108	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs76768877	chr7:100549110-100549111	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs534267105	chr7:100549123-100549124	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs75348441	chr7:100549133-100549134	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs77910748	chr7:100549147-100549148	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs75026765	chr7:100549149-100549150	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs75919307	chr7:100549159-100549160	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs77533482	chr7:100549182-100549183	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs376753678	chr7:100549189-100549190	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs78112056	chr7:100549194-100549195	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs79554433	chr7:100549195-100549196	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs551705358	chr7:100549201-100549202	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs78117209	chr7:100549207-100549208	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs77073976	chr7:100549208-100549209	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs80210479	chr7:100549209-100549210	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs78940807	chr7:100549218-100549219	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs74428330	chr7:100549224-100549225	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs386716145	chr7:100549244-100549245	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs80220736	chr7:100549245-100549246	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs75366089	chr7:100549247-100549248	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs74667171	chr7:100549253-100549254	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs36175019	chr7:100549271-100549272	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs73163747	chr7:100549284-100549285	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs79561223	chr7:100549296-100549297	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs78365737	chr7:100549301-100549302	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs567023302	chr7:100549302-100549303	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs79634497	chr7:100549304-100549305	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs77419249	chr7:100549310-100549311	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs77627097	chr7:100549315-100549316	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:165 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100544800-100550600	Weak transcription	Right Atrium	heart
2	chr7:100546600-100549600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:100546600-100549800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr7:100546800-100549600	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr7:100546800-100549800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr7:100547200-100549800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr7:100547200-100550600	Weak transcription	Gastric	stomach
8	chr7:100547800-100549000	Weak transcription	Spleen	Spleen
9	chr7:100547800-100549600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr7:100547800-100549600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr7:100547800-100549600	Enhancers	H9 Cell Line	embryonic stem cell
12	chr7:100547800-100549600	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr7:100547800-100549600	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr7:100548000-100549600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr7:100548200-100549800	Enhancers	H1 Cell Line	embryonic stem cell
16	chr7:100548400-100549000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr7:100548400-100549400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr7:100548400-100550600	Weak transcription	Liver	Liver
19	chr7:100548400-100550600	Weak transcription	Colonic Mucosa	Colon
20	chr7:100548400-100550600	Strong transcription	Rectal Mucosa Donor 31	rectum
21	chr7:100548600-100549200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr7:100548600-100549200	Active TSS	Fetal Intestine Small	intestine
23	chr7:100548600-100549600	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr7:100548600-100549600	Bivalent Enhancer	Duodenum Mucosa	Duodenum
25	chr7:100548600-100550000	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr7:100548600-100550600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr7:100548600-100550600	Weak transcription	Fetal Intestine Large	intestine
28	chr7:100548600-100550600	Weak transcription	Fetal Thymus	thymus
29	chr7:100548800-100549000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr7:100549000-100549200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr7:100549000-100549400	Enhancers	Spleen	Spleen
32	chr7:100549200-100549400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr7:100549200-100549400	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
34	chr7:100549400-100549600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr7:100549400-100550600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:100549400-100550600	Strong transcription	Fetal Intestine Small	intestine
37	chr7:100549600-100549800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
38	chr7:100549600-100550200	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr7:100549600-100550400	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr7:100549600-100550600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr7:100549600-100550600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr7:100549600-100550600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr7:100549600-100550600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:100549600-100550600	Strong transcription	Duodenum Mucosa	Duodenum
45	chr7:100549600-100551200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr7:100549800-100550200	Weak transcription	Spleen	Spleen
47	chr7:100549800-100550400	Weak transcription	Thymus	Thymus
48	chr7:100549800-100550600	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr7:100549800-100550600	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr7:100549800-100550600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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