Variant report

Variant	esv1835816
Chromosome Location	chr7:103255144-103354223
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:732)
CpG islands
(count:244)
Chromatin interactive
region (count:85)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:103254691-103255182	K562	blood:	n/a	n/a
2	ARID3A	chr7:103298538-103298740	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:103292475-103292581	K562	blood:	n/a	n/a
4	ARID3A	chr7:103300589-103301706	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:103345499-103345520	K562	blood:	n/a	n/a
6	ARID3A	chr7:103305068-103305251	K562	blood:	n/a	n/a
7	ARID3A	chr7:103297830-103298390	K562	blood:	n/a	n/a
8	ARID3A	chr7:103272498-103272859	K562	blood:	n/a	n/a
9	ARID3A	chr7:103319899-103320230	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:103303101-103303301	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:103301632-103301797	K562	blood:	n/a	n/a
12	ARID3A	chr7:103331784-103332058	HepG2	liver:	n/a	n/a
13	ARID3A	chr7:103300792-103301326	K562	blood:	n/a	n/a
14	ATF1	chr7:103297848-103298247	K562	blood:	n/a	n/a
15	ATF1	chr7:103301009-103301317	K562	blood:	n/a	n/a
16	ATF1	chr7:103270803-103271170	K562	blood:	n/a	n/a
17	ATF1	chr7:103272544-103272989	K562	blood:	n/a	n/a
18	ATF1	chr7:103254370-103255262	K562	blood:	n/a	n/a
19	ATF3	chr7:103300900-103301322	K562	blood:	n/a	n/a
20	ATF3	chr7:103297853-103298436	K562	blood:	n/a	n/a
21	ATF3	chr7:103270774-103271095	K562	blood:	n/a	n/a
22	BACH1	chr7:103272623-103272854	K562	blood:	n/a	n/a
23	BCLAF1	chr7:103297809-103298425	K562	blood:	n/a	n/a
24	BHLHE40	chr7:103300942-103301872	K562	blood:	n/a	n/a
25	BHLHE40	chr7:103298944-103299312	K562	blood:	n/a	n/a
26	BHLHE40	chr7:103300881-103301800	HepG2	liver:	n/a	n/a
27	BHLHE40	chr7:103300976-103301276	HepG2	liver:	n/a	n/a
28	BHLHE40	chr7:103297785-103298424	K562	blood:	n/a	n/a
29	BHLHE40	chr7:103298673-103298683	K562	blood:	n/a	n/a
30	BHLHE40	chr7:103297004-103297036	K562	blood:	n/a	n/a
31	BRCA1	chr7:103301680-103301812	GM12878	blood:	n/a	n/a
32	CBX3	chr7:103288018-103288455	K562	blood:	n/a	n/a
33	CBX3	chr7:103321093-103321604	K562	blood:	n/a	n/a
34	CBX3	chr7:103287263-103287578	K562	blood:	n/a	n/a
35	CBX3	chr7:103300852-103301960	K562	blood:	n/a	n/a
36	CBX3	chr7:103284757-103285106	K562	blood:	n/a	n/a
37	CBX3	chr7:103297810-103298390	K562	blood:	n/a	n/a
38	CBX3	chr7:103288516-103288973	K562	blood:	n/a	n/a
39	CBX3	chr7:103254320-103255276	K562	blood:	n/a	n/a
40	CBX3	chr7:103284768-103285082	K562	blood:	n/a	n/a
41	CCNT2	chr7:103301064-103301279	K562	blood:	n/a	n/a
42	CCNT2	chr7:103297868-103298341	K562	blood:	n/a	n/a
43	CCNT2	chr7:103330782-103330935	K562	blood:	n/a	n/a
44	CEBPB	chr7:103308985-103309353	K562	blood:	n/a	chr7:103309158-103309169
45	CEBPB	chr7:103302949-103303079	HepG2	liver:	n/a	n/a
46	CEBPB	chr7:103277585-103277932	Hela-S3	cervix:	n/a	chr7:103277743-103277756
47	CEBPB	chr7:103298583-103298832	K562	blood:	n/a	n/a
48	CEBPB	chr7:103348540-103348769	HepG2	liver:	n/a	chr7:103348647-103348658
49	CEBPB	chr7:103308989-103309336	Hela-S3	cervix:	n/a	chr7:103309158-103309169
50	CEBPB	chr7:103262797-103263107	IMR90	lung:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:103260062-103260112	HMEC	breast:	n/a
2	chr7:103279088-103279138	HepG2	liver:	n/a
3	chr7:103279088-103279138	HCT-116	colon:	n/a
4	chr7:103279088-103279138	HPAEpiC	pulmonary alveolar:	n/a
5	chr7:103301932-103301982	NHDF-neo	bronchial:	n/a
6	chr7:103279088-103279138	U87	brain:	n/a
7	chr7:103343261-103343311	NHDF-neo	bronchial:	n/a
8	chr7:103301932-103301982	SKMC	muscle:	n/a
9	chr7:103279088-103279138	PrEC	prostate:	n/a
10	chr7:103301932-103301982	NH-A	brain:	n/a
11	chr7:103301932-103301982	PANC-1	pancreas:	n/a
12	chr7:103343261-103343311	AG09319	gingival:	n/a
13	chr7:103260062-103260112	K562	blood:	n/a
14	chr7:103343261-103343311	HIPEpiC	eye:	n/a
15	chr7:103260062-103260112	HCF	heart:	n/a
16	chr7:103260062-103260112	AG04450	lung:	fetal
17	chr7:103279088-103279138	GM06990	blood:	n/a
18	chr7:103260062-103260112	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:103301932-103301982	MCF10A-Er-Src	breast:	n/a
20	chr7:103279088-103279138	Hela-S3	cervix:	n/a
21	chr7:103260062-103260112	HEK293	kidney:	embryo
22	chr7:103260062-103260112	AoSMC	blood vessel:	n/a
23	chr7:103279088-103279138	HRPEpiC	eye:	n/a
24	chr7:103260062-103260112	GM12891	blood:	n/a
25	chr7:103343261-103343311	BE2_C	brain:	n/a
26	chr7:103301932-103301982	NT2-D1	testis:	n/a
27	chr7:103301932-103301982	HL-60	blood:	n/a
28	chr7:103343261-103343311	BJ	skin:	n/a
29	chr7:103279088-103279138	AG09319	gingival:	n/a
30	chr7:103260062-103260112	NHDF-neo	bronchial:	n/a
31	chr7:103343261-103343311	T-47D	breast:	n/a
32	chr7:103279088-103279138	PANC-1	pancreas:	n/a
33	chr7:103301932-103301982	SK-N-SH_RA	brain:	n/a
34	chr7:103301932-103301982	NB4	blood:	n/a
35	chr7:103260062-103260112	HIPEpiC	eye:	n/a
36	chr7:103279088-103279138	GM12892	blood:	n/a
37	chr7:103279088-103279138	GM12891	blood:	n/a
38	chr7:103343261-103343311	AG09309	skin:	n/a
39	chr7:103343261-103343311	HRCEpiC	kidney:	n/a
40	chr7:103343261-103343311	HCM	heart:	n/a
41	chr7:103343261-103343311	AG10803	skin:	n/a
42	chr7:103279088-103279138	ECC-1	luminal epithelium:	n/a
43	chr7:103343261-103343311	NHBE	bronchial:	n/a
44	chr7:103301932-103301982	HIPEpiC	eye:	n/a
45	chr7:103279088-103279138	NH-A	brain:	n/a
46	chr7:103301932-103301982	Hela-S3	cervix:	n/a
47	chr7:103279088-103279138	BJ	skin:	n/a
48	chr7:103343261-103343311	Jurkat	blood:	n/a
49	chr7:103279088-103279138	Hepatocyte	liver:	n/a
50	chr7:103260062-103260112	HUVEC	blood vessel:	n/a

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:103282215..103284239-chr7:103291796..103293845,2	K562	blood:
2	chr7:103254361..103256762-chr7:103277435..103279324,2	K562	blood:
3	chr7:103294590..103296926-chr7:103297378..103300214,2	MCF-7	breast:
4	chr7:103305325..103307446-chr7:103308405..103311533,3	K562	blood:
5	chr7:103304565..103307754-chr7:103310017..103312490,3	MCF-7	breast:
6	chr7:103297558..103299544-chr7:103301065..103303822,2	K562	blood:
7	chr7:103274516..103276734-chr7:103323210..103324865,2	K562	blood:
8	chr7:103335628..103338296-chr7:103339379..103341676,2	K562	blood:
9	chr7:103270998..103273560-chr7:103345066..103347137,2	K562	blood:
10	chr7:103331145..103334618-chr7:103343062..103346104,3	K562	blood:
11	chr7:103308135..103310700-chr7:103389205..103391721,2	K562	blood:
12	chr7:103299107..103301619-chr7:103313448..103316125,2	K562	blood:
13	chr7:103319857..103322133-chr7:103324441..103326185,2	K562	blood:
14	chr7:103353358..103354892-chr7:103355779..103358265,2	K562	blood:
15	chr7:103304565..103307754-chr7:103310017..103312490,3	MCF-7	breast:
16	chr7:103270998..103273560-chr7:103345066..103347137,2	K562	blood:
17	chr7:103317265..103318877-chr7:103327937..103330209,2	K562	blood:
18	chr17:62024047..62024737-chr7:103272103..103272828,2	MCF-7	breast:
19	chr7:103331145..103334618-chr7:103343062..103346104,3	K562	blood:
20	chr7:103254507..103256433-chr7:103303415..103304942,2	K562	blood:
21	chr7:103262757..103265718-chr7:103587401..103589902,2	K562	blood:
22	chr7:103253050..103254714-chr7:103265200..103267338,2	MCF-7	breast:
23	chr7:103334750..103336512-chr7:103338855..103341152,3	K562	blood:
24	chr7:103334750..103336512-chr7:103338855..103341152,3	K562	blood:
25	chr7:103298261..103300051-chr7:103303865..103306528,3	K562	blood:
26	chr7:103297764..103300699-chr7:103309943..103311774,3	K562	blood:
27	chr7:103326182..103328296-chr7:103329519..103331647,2	K562	blood:
28	chr7:103313058..103315600-chr7:103766420..103769012,2	K562	blood:
29	chr7:103296674..103299385-chr7:103636597..103638114,2	K562	blood:
30	chr7:103253816..103255808-chr7:103257490..103259015,2	K562	blood:
31	chr7:103346006..103347594-chr7:103348639..103351482,2	MCF-7	breast:
32	chr7:103335628..103338296-chr7:103339379..103341676,2	K562	blood:
33	chr7:103299093..103302989-chr7:103306962..103309461,4	K562	blood:
34	chr7:103317265..103318877-chr7:103327937..103330209,2	K562	blood:
35	chr7:103267673..103270485-chr7:103274294..103276158,2	K562	blood:
36	chr7:103299093..103302989-chr7:103306962..103309461,4	K562	blood:
37	chr7:103294590..103296926-chr7:103297378..103300214,2	MCF-7	breast:
38	chr7:103319857..103322133-chr7:103324441..103326185,2	K562	blood:
39	chr7:103298022..103299710-chr7:103300574..103302831,2	K562	blood:
40	chr7:103254507..103256433-chr7:103303415..103304942,2	K562	blood:
41	chr7:103250881..103252737-chr7:103255714..103258571,2	K562	blood:
42	chr7:103282215..103284239-chr7:103291796..103293845,2	K562	blood:
43	chr7:103267673..103270485-chr7:103274294..103276158,2	K562	blood:
44	chr7:103302157..103305081-chr7:103307428..103309222,2	K562	blood:
45	chr7:103287552..103290222-chr7:103293075..103295780,3	K562	blood:
46	chr7:103254361..103256762-chr7:103277435..103279324,2	K562	blood:
47	chr7:103313587..103316408-chr7:103317847..103320002,2	K562	blood:
48	chr7:103265123..103267515-chr7:103269219..103272108,3	K562	blood:
49	chr7:103348920..103351785-chr7:103353040..103357601,4	K562	blood:
50	chr7:103297074..103301566-chr7:103303216..103306956,8	K562	blood:

No data

Variant related genes	Relation type
RELN	TF binding region
RELN	CpG island
ENSG00000154945	chromatin interactions
ENSG00000189056	chromatin interactions

Extended variants
information (count: 3927 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:3927 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2017179	chr7:103255144-103255145	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs7783216	chr7:103255195-103255196	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs568779481	chr7:103255215-103255216	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs374989712	chr7:103255236-103255237	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs34801423	chr7:103255247-103255248	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs574144787	chr7:103255265-103255266	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs544938628	chr7:103255270-103255271	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs190370538	chr7:103255286-103255287	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs563020450	chr7:103255293-103255294	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs2711841	chr7:103255310-103255311	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs535659488	chr7:103255360-103255361	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs111731320	chr7:103255366-103255367	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs147737214	chr7:103255373-103255374	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs560214756	chr7:103255387-103255388	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs62482566	chr7:103255415-103255416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527736898	chr7:103255478-103255479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181578195	chr7:103255564-103255565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531831443	chr7:103255565-103255566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368726838	chr7:103255582-103255583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537622087	chr7:103255673-103255674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs550082845	chr7:103255681-103255682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540230300	chr7:103255693-103255694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186168454	chr7:103255772-103255773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs553976303	chr7:103255800-103255801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191410928	chr7:103255823-103255824	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs1106655	chr7:103255854-103255855	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs112237442	chr7:103255901-103255902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536389758	chr7:103255908-103255909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565417937	chr7:103255909-103255910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1006817	chr7:103255985-103255986	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs200116608	chr7:103256010-103256011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187777979	chr7:103256039-103256040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141044280	chr7:103256083-103256084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76110142	chr7:103256090-103256091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150235403	chr7:103256109-103256110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189931191	chr7:103256172-103256173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527674776	chr7:103256175-103256176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543134857	chr7:103256223-103256224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561210071	chr7:103256284-103256285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138888879	chr7:103256295-103256296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549682159	chr7:103256315-103256316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149496689	chr7:103256326-103256327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557449191	chr7:103256338-103256339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113079902	chr7:103256371-103256372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371230634	chr7:103256379-103256380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144653601	chr7:103256389-103256390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547707059	chr7:103256403-103256404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2191707	chr7:103256433-103256434	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs535852532	chr7:103256512-103256513	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554685580	chr7:103256515-103256516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	21147910	CNVD
Schizophrenia	23813976	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:304 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103245000-103259600	Weak transcription	HepG2	liver
2	chr7:103253600-103255400	Enhancers	Fetal Heart	heart
3	chr7:103254800-103255200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr7:103255000-103255400	Flanking Active TSS	K562	blood
5	chr7:103255200-103255400	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr7:103255400-103256200	Enhancers	K562	blood
7	chr7:103255800-103256800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr7:103256000-103256800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr7:103256200-103269000	Weak transcription	K562	blood
10	chr7:103256800-103265600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr7:103259600-103260200	Strong transcription	HepG2	liver
12	chr7:103260200-103260400	Enhancers	Stomach Smooth Muscle	stomach
13	chr7:103260200-103267000	Weak transcription	HepG2	liver
14	chr7:103265600-103268400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr7:103266400-103266600	Enhancers	NHLF	lung
16	chr7:103266600-103270800	Weak transcription	NHLF	lung
17	chr7:103266800-103267200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr7:103267000-103267600	Strong transcription	HepG2	liver
19	chr7:103267000-103268000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr7:103267000-103268400	Enhancers	NHDF-Ad	bronchial
21	chr7:103267200-103270800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr7:103267400-103268000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr7:103267600-103270000	Weak transcription	HepG2	liver
24	chr7:103268000-103270600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr7:103268000-103272600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr7:103268400-103270800	Weak transcription	NHDF-Ad	bronchial
27	chr7:103268400-103273600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr7:103269000-103270800	Strong transcription	K562	blood
29	chr7:103270000-103271200	Strong transcription	HepG2	liver
30	chr7:103270600-103271000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr7:103270600-103271200	Enhancers	Muscle Satellite Cultured Cells	--
32	chr7:103270800-103271000	Enhancers	HUVEC	blood vessel
33	chr7:103270800-103271000	Enhancers	NHEK	skin
34	chr7:103270800-103271200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr7:103270800-103271200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr7:103270800-103271200	Enhancers	NH-A	brain
37	chr7:103270800-103271200	Enhancers	NHDF-Ad	bronchial
38	chr7:103270800-103271200	Enhancers	NHLF	lung
39	chr7:103270800-103271400	Genic enhancers	K562	blood
40	chr7:103271000-103271200	Enhancers	HMEC	breast
41	chr7:103271000-103272600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr7:103271200-103272400	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr7:103271200-103272600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr7:103271200-103272600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr7:103271200-103272600	Weak transcription	NH-A	brain
46	chr7:103271200-103275800	Weak transcription	HepG2	liver
47	chr7:103271200-103276800	Weak transcription	NHLF	lung
48	chr7:103271200-103277000	Weak transcription	NHDF-Ad	bronchial
49	chr7:103271400-103272400	Weak transcription	K562	blood
50	chr7:103271400-103272600	Weak transcription	NHEK	skin

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