Variant report

Variant	nsv464418
Chromosome Location	chr7:31072386-31116168
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	BACH1	chr7:31091913-31092230	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:31100886-31101125	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr7:31101043-31101083	K562	blood:	n/a	n/a
4	BHLHE40	chr7:31100779-31100785	K562	blood:	n/a	n/a
5	CEBPB	chr7:31101647-31101955	A549	lung:	n/a	n/a
6	CEBPB	chr7:31103041-31103259	IMR90	lung:	n/a	chr7:31103158-31103169
7	CEBPB	chr7:31103006-31103237	HepG2	liver:	n/a	chr7:31103158-31103169
8	CEBPB	chr7:31102996-31103288	A549	lung:	n/a	chr7:31103158-31103169
9	CEBPB	chr7:31101730-31101916	HepG2	liver:	n/a	n/a
10	CEBPB	chr7:31103031-31103286	Hela-S3	cervix:	n/a	chr7:31103158-31103169
11	CEBPB	chr7:31099407-31099455	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr7:31099265-31099437	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr7:31082649-31083031	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr7:31093219-31093443	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr7:31099240-31099390	Hela-S3	cervix:	n/a	chr7:31099357-31099370 chr7:31099354-31099372
16	CTCF	chr7:31105022-31105124	GM19238	blood:	n/a	n/a
17	CTCF	chr7:31100980-31101130	GM12868	blood:	n/a	chr7:31101033-31101042
18	CTCF	chr7:31100960-31101110	GM12866	blood:	n/a	chr7:31101033-31101042
19	CTCF	chr7:31099300-31099450	K562	blood:	n/a	chr7:31099357-31099370 chr7:31099354-31099372
20	CTCF	chr7:31096403-31096656	H1-hESC	embryonic stem cell:	n/a	chr7:31096533-31096543
21	CTCF	chr7:31100920-31101070	NB4	blood:	n/a	chr7:31101033-31101042
22	CTCF	chr7:31100734-31101318	K562	blood:	n/a	chr7:31101033-31101042
23	CTCF	chr7:31099284-31099410	MCF-7	breast:	n/a	chr7:31099357-31099370 chr7:31099354-31099372
24	CTCF	chr7:31100960-31101110	GM12875	blood:	n/a	chr7:31101033-31101042
25	CTCF	chr7:31079900-31080050	MCF-7	breast:	n/a	chr7:31079997-31080010 chr7:31079990-31080011
26	CTCF	chr7:31096424-31096695	MCF-7	breast:	n/a	chr7:31096533-31096543
27	CTCF	chr7:31099215-31099472	K562	blood:	n/a	chr7:31099357-31099370 chr7:31099354-31099372
28	CTCF	chr7:31100980-31101130	HMF	breast:	n/a	chr7:31101033-31101042
29	CTCF	chr7:31100900-31101050	A549	lung:	n/a	chr7:31101033-31101042
30	CTCF	chr7:31096400-31096550	WERI-Rb-1	eye:	n/a	chr7:31096533-31096543
31	CTCF	chr7:31104940-31105090	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr7:31101000-31101150	MCF-7	breast:	n/a	chr7:31101033-31101042
33	CTCF	chr7:31091904-31092080	Fibrobl	skin:	n/a	chr7:31091972-31091985
34	CTCF	chr7:31100940-31101090	HepG2	liver:	n/a	chr7:31101033-31101042
35	CTCF	chr7:31100935-31101160	K562	blood:	n/a	chr7:31101033-31101042
36	CTCF	chr7:31096980-31097130	HRE	kidney:	n/a	n/a
37	CTCF	chr7:31096520-31096594	GM10248	blood:	n/a	chr7:31096533-31096543
38	CTCF	chr7:31099340-31099490	GM12871	blood:	n/a	chr7:31099357-31099370 chr7:31099354-31099372
39	CTCF	chr7:31096483-31096596	LNCaP	prostate:	n/a	chr7:31096533-31096543
40	CTCF	chr7:31099200-31099350	HRE	kidney:	n/a	n/a
41	CTCF	chr7:31096436-31096647	A549	lung:	n/a	chr7:31096533-31096543
42	CTCF	chr7:31100900-31101050	WERI-Rb-1	eye:	n/a	chr7:31101033-31101042
43	CTCF	chr7:31091880-31092030	WERI-Rb-1	eye:	n/a	chr7:31091972-31091985
44	CTCF	chr7:31096500-31096650	NB4	blood:	n/a	chr7:31096533-31096543
45	CTCF	chr7:31096480-31096630	RPTEC	kidney:	n/a	chr7:31096533-31096543
46	CTCF	chr7:31092021-31092030	NHEK	skin:	n/a	n/a
47	CTCF	chr7:31096460-31096610	K562	blood:	n/a	chr7:31096533-31096543
48	CTCF	chr7:31099296-31099390	GM12892	blood:	n/a	chr7:31099357-31099370 chr7:31099354-31099372
49	CTCF	chr7:31100900-31101050	GM12874	blood:	n/a	chr7:31101033-31101042
50	CTCF	chr7:31099300-31099450	A549	lung:	n/a	chr7:31099357-31099370 chr7:31099354-31099372

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:31099814-31099864	HPAEpiC	pulmonary alveolar:	n/a
2	chr7:31107864-31107914	NB4	blood:	n/a
3	chr7:31091718-31091768	GM06990	blood:	n/a
4	chr7:31093176-31093226	LNCaP	prostate:	n/a
5	chr7:31091718-31091768	NB4	blood:	n/a
6	chr7:31089142-31089192	NHBE	bronchial:	n/a
7	chr7:31082763-31082813	LNCaP	prostate:	n/a
8	chr7:31101520-31101570	Jurkat	blood:	n/a
9	chr7:31093176-31093226	HCT-116	colon:	n/a
10	chr7:31091718-31091768	BJ	skin:	n/a
11	chr7:31091718-31091768	GM19239	blood:	n/a
12	chr7:31099814-31099864	HCT-116	colon:	n/a
13	chr7:31102195-31102245	PrEC	prostate:	n/a
14	chr7:31091813-31091863	BJ	skin:	n/a
15	chr7:31096717-31096767	HCPEpiC	choroid plexus:	n/a
16	chr7:31091825-31091875	GM12891	blood:	n/a
17	chr7:31091813-31091863	PrEC	prostate:	n/a
18	chr7:31089142-31089192	HCPEpiC	choroid plexus:	n/a
19	chr7:31092970-31093020	HNPCEpiC	eye:	n/a
20	chr7:31096717-31096767	HMEC	breast:	n/a
21	chr7:31091813-31091863	Hepatocyte	liver:	n/a
22	chr7:31092854-31092904	HRE	kidney:	n/a
23	chr7:31091813-31091863	NHDF-neo	bronchial:	n/a
24	chr7:31092589-31092639	HL-60	blood:	n/a
25	chr7:31091813-31091863	HepG2	liver:	n/a
26	chr7:31099814-31099864	MCF-7	breast:	n/a
27	chr7:31091245-31091295	ProgFib	skin:	n/a
28	chr7:31092589-31092639	MCF-7	breast:	n/a
29	chr7:31091813-31091863	AoSMC	blood vessel:	n/a
30	chr7:31091813-31091863	MCF10A-Er-Src	breast:	n/a
31	chr7:31093176-31093226	U87	brain:	n/a
32	chr7:31102195-31102245	GM12878	blood:	n/a
33	chr7:31092854-31092904	HCT-116	colon:	n/a
34	chr7:31091813-31091863	Hela-S3	cervix:	n/a
35	chr7:31091813-31091863	HRPEpiC	eye:	n/a
36	chr7:31091825-31091875	Hela-S3	cervix:	n/a
37	chr7:31091718-31091768	AG09319	gingival:	n/a
38	chr7:31091718-31091768	HRE	kidney:	n/a
39	chr7:31102195-31102245	NB4	blood:	n/a
40	chr7:31091718-31091768	HRCEpiC	kidney:	n/a
41	chr7:31102195-31102245	PFSK-1	brain:	n/a
42	chr7:31091718-31091768	A549	lung:	n/a
43	chr7:31101520-31101570	T-47D	breast:	n/a
44	chr7:31092589-31092639	A549	lung:	n/a
45	chr7:31092970-31093020	NHBE	bronchial:	n/a
46	chr7:31092589-31092639	HEEpiC	esophagus:	n/a
47	chr7:31091718-31091768	HMEC	breast:	n/a
48	chr7:31099814-31099864	HEEpiC	esophagus:	n/a
49	chr7:31089142-31089192	HCF	heart:	n/a
50	chr7:31091718-31091768	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:31068808..31070326-chr7:31073599..31075373,2	K562	blood:
2	chr7:31023139..31023844-chr7:31095798..31096741,4	MCF-7	breast:
3	chr7:31103676..31106602-chr7:31108175..31110315,2	MCF-7	breast:
4	chr7:31086642..31089311-chr7:31093332..31095013,2	MCF-7	breast:
5	chr7:31022941..31023450-chr7:31098892..31099640,2	MCF-7	breast:
6	chr7:31098225..31100619-chr7:31102389..31105228,2	K562	blood:
7	chr7:31023222..31023904-chr7:31079893..31080446,2	MCF-7	breast:
8	chr7:31091380..31093823-chr7:31094980..31097545,2	MCF-7	breast:
9	chr7:31096673..31098755-chr7:31119643..31122776,3	K562	blood:
10	chr7:31100626..31101458-chr7:31162309..31162915,2	K562	blood:
11	chr7:31064780..31067047-chr7:31094437..31096416,2	K562	blood:
12	chr7:31075786..31080019-chr7:31080781..31086133,6	K562	blood:
13	chr7:31099278..31099779-chr7:31154728..31155481,2	K562	blood:
14	chr7:31068826..31070596-chr7:31073599..31075354,2	K562	blood:
15	chr7:31075786..31080019-chr7:31080781..31086133,6	K562	blood:
16	chr7:31031861..31034670-chr7:31076985..31078607,2	K562	blood:
17	chr7:31078397..31080821-chr7:31091152..31094315,3	MCF-7	breast:
18	chr7:31086642..31089311-chr7:31093332..31095013,2	MCF-7	breast:
19	chr7:31103676..31106602-chr7:31108175..31110315,2	MCF-7	breast:
20	chr7:31091380..31093823-chr7:31094980..31097545,2	MCF-7	breast:

Variant related genes	Relation type
ADCYAP1R1	TF binding region
ADCYAP1R1	CpG island
ENSG00000106128	chromatin interactions
ENSG00000078549	chromatin interactions

Extended variants
information (count: 1663 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1663 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12111795	chr7:31072386-31072387	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566490617	chr7:31072396-31072397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185197332	chr7:31072445-31072446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34548976	chr7:31072469-31072470	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs576972676	chr7:31072470-31072471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531389939	chr7:31072473-31072474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs79405186	chr7:31072500-31072501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556370098	chr7:31072514-31072515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142829127	chr7:31072536-31072537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557933767	chr7:31072564-31072565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542139974	chr7:31072573-31072574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73088268	chr7:31072588-31072589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs577813885	chr7:31072597-31072598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147399524	chr7:31072618-31072619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs35345343	chr7:31072642-31072643	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs189568071	chr7:31072693-31072694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532518384	chr7:31072699-31072700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs568044252	chr7:31072744-31072745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550777432	chr7:31072781-31072782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563132928	chr7:31072809-31072810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs73309733	chr7:31072817-31072818	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs557153232	chr7:31072827-31072828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs548885731	chr7:31072867-31072868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs34553505	chr7:31072874-31072875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183353917	chr7:31072877-31072878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs533780230	chr7:31072908-31072909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188581240	chr7:31072962-31072963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570458835	chr7:31072977-31072978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs537974394	chr7:31073041-31073042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs1894846	chr7:31073054-31073055	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs1894845	chr7:31073063-31073064	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs559655494	chr7:31073113-31073114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs553652910	chr7:31073121-31073122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191910240	chr7:31073137-31073138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs11979615	chr7:31073143-31073144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535507603	chr7:31073147-31073148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs6976040	chr7:31073152-31073153	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs59676783	chr7:31073176-31073177	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs544709771	chr7:31073186-31073187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs11972834	chr7:31073217-31073218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530319378	chr7:31073260-31073261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs138088642	chr7:31073270-31073271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs58828910	chr7:31073365-31073366	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs188647322	chr7:31073411-31073412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs75681217	chr7:31073418-31073419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191869936	chr7:31073423-31073424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs143541687	chr7:31073476-31073477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs6980078	chr7:31073495-31073496	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs75326371	chr7:31073519-31073520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535645705	chr7:31073541-31073542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	22522925	CNVD
Colorectal cancer	21645411	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:639 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:31063400-31086800	Weak transcription	Spleen	Spleen
2	chr7:31067600-31082400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:31069400-31076600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:31070200-31082600	Weak transcription	Fetal Brain Male	brain
5	chr7:31070400-31072600	Weak transcription	Fetal Muscle Leg	muscle
6	chr7:31070400-31072800	Weak transcription	Fetal Muscle Trunk	muscle
7	chr7:31072600-31074200	Enhancers	Fetal Muscle Leg	muscle
8	chr7:31072800-31074400	Enhancers	Fetal Muscle Trunk	muscle
9	chr7:31073000-31073200	Enhancers	Psoas Muscle	Psoas
10	chr7:31073400-31073600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:31074200-31075400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr7:31074400-31074600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr7:31074400-31074600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:31074400-31075000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr7:31074600-31074800	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr7:31075400-31076400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr7:31076400-31076600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr7:31076600-31076800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr7:31076800-31082600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr7:31077200-31077800	Enhancers	Brain Angular Gyrus	brain
21	chr7:31077800-31081800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr7:31080200-31081000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr7:31080600-31081000	Enhancers	NHDF-Ad	bronchial
24	chr7:31080600-31082200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr7:31080800-31081000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr7:31081200-31082000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
27	chr7:31081400-31082600	Enhancers	H9 Cell Line	embryonic stem cell
28	chr7:31081800-31082000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
29	chr7:31081800-31082000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr7:31081800-31082600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr7:31081800-31082800	Bivalent Enhancer	Fetal Muscle Leg	muscle
32	chr7:31081800-31085000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr7:31082000-31082400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr7:31082000-31082600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr7:31082000-31085000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr7:31082000-31085000	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr7:31082200-31082400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
38	chr7:31082200-31082600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr7:31082200-31083000	Bivalent Enhancer	Fetal Stomach	stomach
40	chr7:31082200-31083600	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr7:31082200-31084400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr7:31082200-31084400	Enhancers	Brain Germinal Matrix	brain
43	chr7:31082200-31085200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr7:31082400-31082800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
45	chr7:31082400-31082800	Bivalent Enhancer	Placenta	Placenta
46	chr7:31082400-31083000	Enhancers	Ovary	ovary
47	chr7:31082400-31083600	Enhancers	H1 Cell Line	embryonic stem cell
48	chr7:31082400-31085000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr7:31082400-31085200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr7:31082600-31082800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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