Variant report

Variant	nsv508694
Chromosome Location	chr1:216901014-216923883
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	CEBPB	chr1:216905083-216905276	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr1:216923509-216923709	IMR90	lung:	n/a	n/a
3	CEBPB	chr1:216905500-216905851	HepG2	liver:	n/a	chr1:216905667-216905678
4	CEBPB	chr1:216918844-216919532	HepG2	liver:	n/a	chr1:216919431-216919444 chr1:216919433-216919442 chr1:216919433-216919442 chr1:216919433-216919442 chr1:216919431-216919442 chr1:216919433-216919442
5	CTCF	chr1:216916100-216916250	GM12864	blood:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183
6	CTCF	chr1:216916080-216916230	HA-sp	spinal cord:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183
7	CTCF	chr1:216923520-216923670	SAEC	small airway:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
8	CTCF	chr1:216916080-216916230	HPAF	blood vessel:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183
9	CTCF	chr1:216923440-216923590	HCM	heart:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
10	CTCF	chr1:216923480-216923630	GM12870	blood:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
11	CTCF	chr1:216916100-216916250	NHDF-neo	bronchial:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183
12	CTCF	chr1:216923365-216923752	GM12878	blood:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
13	CTCF	chr1:216923480-216923630	AG10803	skin:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
14	CTCF	chr1:216923460-216923610	AG04449	skin:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
15	CTCF	chr1:216923380-216923530	HAc	cerebellar:	n/a	n/a
16	CTCF	chr1:216923500-216923650	GM12869	blood:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
17	CTCF	chr1:216923500-216923650	HUVEC	blood vessel:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
18	CTCF	chr1:216916100-216916250	AG10803	skin:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183
19	CTCF	chr1:216923480-216923630	NHLF	lung:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
20	CTCF	chr1:216923480-216923630	GM12869	blood:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
21	CTCF	chr1:216923460-216923610	HA-sp	spinal cord:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
22	CTCF	chr1:216916060-216916210	HEK293	kidney:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183
23	CTCF	chr1:216923500-216923650	SK-N-SH_RA	brain:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
24	CTCF	chr1:216923480-216923630	HMEC	breast:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
25	CTCF	chr1:216916100-216916250	AG09319	gingival:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183
26	CTCF	chr1:216916100-216916250	A549	lung:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183
27	CTCF	chr1:216923529-216923608	GM12891	blood:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
28	CTCF	chr1:216923480-216923630	GM12865	blood:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
29	CTCF	chr1:216916020-216916170	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr1:216923441-216923672	HUVEC	blood vessel:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
31	CTCF	chr1:216923460-216923610	GM12870	blood:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
32	CTCF	chr1:216916090-216916249	Hela-S3	cervix:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183
33	CTCF	chr1:216923415-216923670	Pancreas_OC	pancreas:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
34	CTCF	chr1:216916160-216916310	BJ	skin:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183
35	CTCF	chr1:216916100-216916250	HCM	heart:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183
36	CTCF	chr1:216923480-216923630	GM12871	blood:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
37	CTCF	chr1:216916076-216916257	GM12878	blood:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183
38	CTCF	chr1:216923426-216923676	Hela-S3	cervix:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
39	CTCF	chr1:216923500-216923650	GM12872	blood:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
40	CTCF	chr1:216923403-216923706	Gliobla	brain:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
41	CTCF	chr1:216916160-216916310	HMF	breast:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183
42	CTCF	chr1:216923480-216923630	GM12872	blood:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
43	CTCF	chr1:216915968-216916317	H1-hESC	embryonic stem cell:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183
44	CTCF	chr1:216916120-216916270	Caco-2	colon:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183
45	CTCF	chr1:216916078-216916306	MCF-7	breast:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183
46	CTCF	chr1:216916115-216916216	HepG2	liver:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183
47	CTCF	chr1:216916007-216916289	SK-N-SH_RA	brain:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183
48	CTCF	chr1:216923480-216923630	HVMF	connective:	n/a	chr1:216923548-216923566 chr1:216923549-216923565 chr1:216923550-216923571
49	CTCF	chr1:216916120-216916270	HMEC	breast:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183
50	CTCF	chr1:216916100-216916250	HEEpiC	esophagus:	n/a	chr1:216916166-216916184 chr1:216916169-216916179 chr1:216916161-216916182 chr1:216916167-216916183

No.	Distal block	Cell Line	Cell type
1	chr1:216922971..216923671-chr1:217505833..217506672,3	MCF-7	breast:
2	chr1:216901271..216903565-chr1:216909673..216911332,2	K562	blood:
3	chr1:216774056..216774839-chr1:216915422..216916227,3	MCF-7	breast:
4	chr1:216901271..216903565-chr1:216909673..216911332,2	K562	blood:
5	chr1:216483863..216484806-chr1:216915394..216916440,4	MCF-7	breast:
6	chr1:216906643..216908171-chr1:216912296..216914026,2	K562	blood:
7	chr1:216913983..216915914-chr1:216921531..216923998,2	MCF-7	breast:
8	chr1:216898478..216901280-chr17:38145496..38147429,2	MCF-7	breast:
9	chr1:216913983..216915914-chr1:216921531..216923998,2	MCF-7	breast:
10	chr1:216739906..216740741-chr1:216915729..216916621,3	MCF-7	breast:
11	chr1:216906643..216908171-chr1:216912296..216914026,2	K562	blood:
12	chr1:216913734..216915380-chr1:216918408..216920801,2	MCF-7	breast:
13	chr1:216923084..216923982-chr1:217507003..217507840,6	MCF-7	breast:
14	chr1:216914787..216915287-chr19:51522088..51522734,2	HCT-116	colon:
15	chr1:216913734..216915380-chr1:216918408..216920801,2	MCF-7	breast:
16	chr1:215997510..215998170-chr1:216923482..216924060,2	MCF-7	breast:
17	chr1:216285193..216285790-chr1:216916011..216916615,2	MCF-7	breast:
18	chr1:216739958..216740765-chr1:216915802..216916535,2	MCF-7	breast:

Variant related genes	Relation type
ESRRG	TF binding region
ENSG00000129451	chromatin interactions

Extended variants
information (count: 917 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146447573	chr1:216901026-216901027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs140874701	chr1:216901063-216901064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541669202	chr1:216901064-216901065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542030407	chr1:216901095-216901096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555926479	chr1:216901107-216901108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561832986	chr1:216901109-216901110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527605939	chr1:216901111-216901112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201214265	chr1:216901155-216901156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541365282	chr1:216901193-216901194	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs113165319	chr1:216901244-216901245	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs564360201	chr1:216901247-216901248	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs187502897	chr1:216901252-216901253	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs144612362	chr1:216901277-216901278	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs373075157	chr1:216901283-216901284	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs77302796	chr1:216901320-216901321	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs528940668	chr1:216901326-216901327	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs549179120	chr1:216901338-216901339	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs547629569	chr1:216901388-216901389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs4503415	chr1:216901389-216901390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564474499	chr1:216901433-216901434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138506762	chr1:216901477-216901478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371482111	chr1:216901500-216901501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534866402	chr1:216901625-216901626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11572661	chr1:216901658-216901659	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs533133614	chr1:216901679-216901680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546093898	chr1:216901683-216901684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571898818	chr1:216901701-216901702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs36016530	chr1:216901759-216901760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1416618	chr1:216901760-216901761	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs574067998	chr1:216901849-216901850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181627779	chr1:216901850-216901851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs72737401	chr1:216901856-216901857	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs572307209	chr1:216901882-216901883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368282286	chr1:216901888-216901889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs17041488	chr1:216901932-216901933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564421817	chr1:216901937-216901938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150270641	chr1:216901944-216901945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370834333	chr1:216901951-216901952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12144183	chr1:216901955-216901956	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs563259725	chr1:216901968-216901969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528998742	chr1:216902004-216902005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376006765	chr1:216902039-216902040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567374142	chr1:216902067-216902068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548693959	chr1:216902081-216902082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138913477	chr1:216902119-216902120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528701036	chr1:216902142-216902143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs72737402	chr1:216902151-216902152	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs550216988	chr1:216902173-216902174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571850122	chr1:216902177-216902178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570125604	chr1:216902211-216902212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Pleomorphic liposarcoma	18784837	CNVD

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:216897400-216901400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:216897400-216958600	Weak transcription	Pancreas	Pancrea
3	chr1:216903200-216903400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:216903400-216904800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:216904600-216904800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr1:216904600-216905000	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr1:216904600-216905200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr1:216904600-216905200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr1:216904800-216905200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr1:216904800-216905200	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr1:216904800-216905200	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr1:216904800-216905200	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr1:216904800-216905200	Enhancers	Fetal Heart	heart
14	chr1:216904800-216905400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr1:216905200-216909800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr1:216905200-216913200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:216907400-216913400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr1:216909800-216910400	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr1:216910000-216911600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr1:216910400-216911800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr1:216911000-216911200	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr1:216911200-216911800	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr1:216911200-216912400	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr1:216911600-216934200	Weak transcription	Psoas Muscle	Psoas
25	chr1:216911800-216912200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr1:216911800-216913000	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr1:216911800-216913000	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr1:216912000-216913000	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr1:216912200-216912400	Enhancers	H1 Cell Line	embryonic stem cell
30	chr1:216912200-216912800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr1:216912200-216913000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr1:216912200-216914400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr1:216912400-216913000	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr1:216912400-216913000	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr1:216912600-216914000	Enhancers	Fetal Heart	heart
36	chr1:216912800-216913000	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr1:216912800-216913200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr1:216912800-216913400	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr1:216912800-216913800	Enhancers	H9 Cell Line	embryonic stem cell
40	chr1:216912800-216914400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr1:216913000-216913200	Enhancers	H1 Cell Line	embryonic stem cell
42	chr1:216913000-216913400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr1:216913000-216913400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr1:216913000-216913800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
45	chr1:216913000-216913800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
46	chr1:216913000-216914000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
47	chr1:216913000-216914200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
48	chr1:216913000-216914400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
49	chr1:216913200-216913400	Flanking Active TSS	H1 Cell Line	embryonic stem cell
50	chr1:216913200-216913400	Active TSS	iPS-20b Cell Line	embryonic stem cell

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