Variant report

Variant	esv2751286
Chromosome Location	chr14:83066038-83203657
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	BHLHE40	chr14:83118887-83118971	A549	lung:	n/a	n/a
2	CBX3	chr14:83176601-83176841	K562	blood:	n/a	n/a
3	CEBPB	chr14:83155377-83155533	A549	lung:	n/a	chr14:83155487-83155500 chr14:83155487-83155500
4	CEBPB	chr14:83142772-83143116	A549	lung:	n/a	chr14:83142938-83142949
5	CEBPB	chr14:83107538-83107864	IMR90	lung:	n/a	chr14:83107714-83107727 chr14:83107716-83107727 chr14:83107660-83107669 chr14:83107658-83107669 chr14:83107658-83107671 chr14:83107716-83107725
6	CEBPB	chr14:83065879-83066158	HepG2	liver:	n/a	chr14:83066019-83066030
7	CEBPB	chr14:83083006-83083329	HepG2	liver:	n/a	chr14:83083147-83083158
8	CEBPB	chr14:83142902-83143069	K562	blood:	n/a	chr14:83142938-83142949
9	CEBPB	chr14:83079406-83079669	A549	lung:	n/a	n/a
10	CEBPB	chr14:83176602-83176850	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr14:83156316-83156629	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr14:83142772-83143120	IMR90	lung:	n/a	chr14:83142938-83142949
13	CEBPB	chr14:83065935-83066143	A549	lung:	n/a	chr14:83066019-83066030
14	CEBPB	chr14:83156460-83156535	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr14:83107545-83107857	HepG2	liver:	n/a	chr14:83107714-83107727 chr14:83107716-83107727 chr14:83107660-83107669 chr14:83107658-83107669 chr14:83107658-83107671 chr14:83107716-83107725
16	CEBPB	chr14:83142779-83143130	HepG2	liver:	n/a	chr14:83142938-83142949
17	CEBPB	chr14:83107565-83107829	A549	lung:	n/a	chr14:83107714-83107727 chr14:83107716-83107727 chr14:83107660-83107669 chr14:83107658-83107669 chr14:83107658-83107671 chr14:83107716-83107725
18	CEBPB	chr14:83170636-83170898	A549	lung:	n/a	n/a
19	CEBPB	chr14:83083056-83083263	H1-hESC	embryonic stem cell:	n/a	chr14:83083147-83083158
20	CTCF	chr14:83176700-83176850	BE2_C	brain:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
21	CTCF	chr14:83176340-83176490	HPF	lung:	n/a	n/a
22	CTCF	chr14:83088540-83088690	GM12872	blood:	n/a	n/a
23	CTCF	chr14:83176720-83176870	GM12869	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
24	CTCF	chr14:83176660-83176810	BE2_C	brain:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
25	CTCF	chr14:83176557-83177075	MCF-7	breast:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
26	CTCF	chr14:83176700-83176850	GM12867	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
27	CTCF	chr14:83176569-83176997	GM12878	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
28	CTCF	chr14:83176700-83176850	SK-N-SH_RA	brain:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
29	CTCF	chr14:83176700-83176850	HMF	breast:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
30	CTCF	chr14:83176666-83176888	GM10248	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
31	CTCF	chr14:83176667-83176905	MCF-7	breast:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
32	CTCF	chr14:83088420-83088570	MCF-7	breast:	n/a	n/a
33	CTCF	chr14:83176625-83176931	MCF-7	breast:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
34	CTCF	chr14:83184590-83184647	GM20000	blood:	n/a	n/a
35	CTCF	chr14:83176700-83176850	GM12864	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
36	CTCF	chr14:83176700-83176850	SAEC	small airway:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
37	CTCF	chr14:83176720-83176870	GM12873	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
38	CTCF	chr14:83176680-83176830	GM12866	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
39	CTCF	chr14:83176640-83176790	RPTEC	kidney:	n/a	chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
40	CTCF	chr14:83176668-83176893	Lung_OC	lung:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
41	CTCF	chr14:83176720-83176870	AG09309	skin:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
42	CTCF	chr14:83176340-83176490	HCM	heart:	n/a	n/a
43	CTCF	chr14:83176700-83176850	GM12878	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
44	CTCF	chr14:83088540-83088690	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr14:83176720-83176870	HUVEC	blood vessel:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
46	CTCF	chr14:83176636-83176924	Medullo	brain:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
47	CTCF	chr14:83176620-83176770	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr14:83088480-83088630	Caco-2	colon:	n/a	n/a
49	CTCF	chr14:83176720-83176870	AG10803	skin:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
50	CTCF	chr14:83176680-83176830	GM12878	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788

No.	Distal block	Cell Line	Cell type
1	chr14:83192387..83194148-chr14:83198757..83201171,2	K562	blood:
2	chr14:83161282..83164222-chr14:83165028..83167917,2	K562	blood:
3	chr14:83176665..83177254-chr14:86523440..86523991,2	MCF-7	breast:
4	chr14:83176690..83177254-chr14:86521578..86522506,2	MCF-7	breast:
5	chr14:83176409..83177253-chr14:83537916..83538885,7	MCF-7	breast:
6	chr14:83176300..83176864-chr14:83537974..83538513,2	MCF-7	breast:
7	chr14:83161282..83164222-chr14:83165028..83167917,2	K562	blood:
8	chr14:83176444..83177428-chr14:86521944..86522598,2	MCF-7	breast:
9	chr14:83192387..83194148-chr14:83198757..83201171,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSHR-5	chr14:83153658-83153714	ENSG00000258743
2	lnc-TSHR-5	chr14:83117268-83118001	ENSG00000258743
3	lnc-TSHR-5	chr14:83161134-83161212	ENSG00000258743
4	lnc-TSHR-5	chr14:83117268-83117340	ENSG00000258743
5	lnc-TSHR-5	chr14:83108882-83109018	NONHSAT038084
6	lnc-TSHR-5	chr14:83153658-83153713	ENSG00000258743
7	lnc-TSHR-5	chr14:83117267-83117334	NONHSAT038084
8	lnc-TSHR-5	chr14:83117268-83117334	XLOC_010887
9	lnc-TSHR-5	chr14:83108980-83109018	ENSG00000258743
10	lnc-TSHR-5	chr14:83108964-83109018	ENSG00000258743
11	lnc-TSHR-5	chr14:83115921-83116488	NONHSAT038089
12	lnc-TSHR-5	chr14:83117268-83117971	NONHSAT038089
13	lnc-TSHR-5	chr14:83108971-83109018	ENSG00000258743
14	lnc-TSHR-5	chr14:83123459-83124110	ENSG00000258743
15	lnc-TSHR-5	chr14:83173045-83173169	ENSG00000258743
16	lnc-TSHR-5	chr14:83108883-83109018	XLOC_010887
17	lnc-TSHR-5	chr14:83117268-83117340	ENSG00000258743
18	lnc-TSHR-5	chr14:83117268-83117340	ENSG00000258743
19	lnc-TSHR-5	chr14:83108976-83109018	ENSG00000258743
20	lnc-TSHR-5	chr14:83151724-83151775	ENSG00000258743

Variant related genes	Relation type
ENSAP2	TF binding region
ENSG00000258743	TF binding region

Extended variants
information (count: 1334 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1334 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374517769	chr14:83077018-83077019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs538170011	chr14:83077066-83077067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182943955	chr14:83077075-83077076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs10137929	chr14:83077109-83077110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139172322	chr14:83077144-83077145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150043665	chr14:83077166-83077167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs144330785	chr14:83077217-83077218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148808257	chr14:83077242-83077243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs372295144	chr14:83077263-83077264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7157338	chr14:83077272-83077273	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs7157030	chr14:83077296-83077297	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs541264673	chr14:83077304-83077305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543967492	chr14:83077307-83077308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs75695574	chr14:83077355-83077356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs74951789	chr14:83077368-83077369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs7157219	chr14:83077380-83077381	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs142457540	chr14:83077406-83077407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530253708	chr14:83077418-83077419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147945038	chr14:83077445-83077446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs141556080	chr14:83077512-83077513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537662779	chr14:83077519-83077520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549910056	chr14:83077571-83077572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530834020	chr14:83077593-83077594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs534019020	chr14:83088611-83088612	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs372098852	chr14:83088714-83088715	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs74908899	chr14:83088775-83088776	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs574567771	chr14:83088802-83088803	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs541971972	chr14:83088821-83088822	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs373795350	chr14:83088846-83088847	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs555253075	chr14:83088864-83088865	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs557299943	chr14:83088923-83088924	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs575561254	chr14:83088925-83088926	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs558099166	chr14:83088960-83088961	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs2798378	chr14:83089024-83089025	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs140726142	chr14:83089045-83089046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs367604373	chr14:83089053-83089054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs117519326	chr14:83089064-83089065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539932684	chr14:83089094-83089095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75363076	chr14:83089098-83089099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529480188	chr14:83089102-83089103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574588152	chr14:83089103-83089104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550722352	chr14:83089108-83089109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192916558	chr14:83089134-83089135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374484032	chr14:83092024-83092025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs368757276	chr14:83092039-83092040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs538710367	chr14:83092071-83092072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs73360736	chr14:83092129-83092130	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs191243770	chr14:83092139-83092140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141428796	chr14:83092166-83092167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181813196	chr14:83092206-83092207	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:133 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:83077000-83077400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr14:83077200-83077600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr14:83077200-83077600	Enhancers	NHEK	skin
4	chr14:83088600-83088800	Active TSS	ES-I3 Cell Line	embryonic stem cell
5	chr14:83088800-83089000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr14:83089000-83089200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr14:83092000-83093400	Enhancers	Brain Cingulate Gyrus	brain
8	chr14:83092400-83093000	Active TSS	Brain Anterior Caudate	brain
9	chr14:83092400-83093200	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr14:83092600-83093000	Enhancers	Brain Angular Gyrus	brain
11	chr14:83092600-83093200	Active TSS	Brain Hippocampus Middle	brain
12	chr14:83092600-83093400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr14:83092800-83093000	Flanking Active TSS	Brain Substantia Nigra	brain
14	chr14:83093000-83093200	Active TSS	Brain Substantia Nigra	brain
15	chr14:83093200-83093400	Flanking Active TSS	Brain Hippocampus Middle	brain
16	chr14:83093200-83093400	Flanking Active TSS	Brain Substantia Nigra	brain
17	chr14:83093400-83093800	Enhancers	Brain Hippocampus Middle	brain
18	chr14:83093400-83093800	Enhancers	Brain Substantia Nigra	brain
19	chr14:83098600-83099400	Enhancers	Stomach Smooth Muscle	stomach
20	chr14:83108400-83109800	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr14:83108400-83110200	Active TSS	iPS-15b Cell Line	embryonic stem cell
22	chr14:83108400-83110400	Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr14:83108600-83109200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
24	chr14:83108600-83109200	Active TSS	Fetal Muscle Leg	muscle
25	chr14:83108600-83109200	Active TSS	A549	lung
26	chr14:83108600-83109400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr14:83108600-83109400	Active TSS	Brain Germinal Matrix	brain
28	chr14:83108600-83109400	Active TSS	Fetal Intestine Large	intestine
29	chr14:83108600-83109400	Active TSS	Fetal Stomach	stomach
30	chr14:83108600-83110200	Active TSS	HUES48 Cell Line	embryonic stem cell
31	chr14:83108800-83109200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr14:83108800-83109200	Active TSS	Duodenum Smooth Muscle	Duodenum
33	chr14:83108800-83109200	Active TSS	Fetal Brain Female	brain
34	chr14:83108800-83109200	Active TSS	Fetal Muscle Trunk	muscle
35	chr14:83108800-83109200	Active TSS	Ovary	ovary
36	chr14:83108800-83109200	Active TSS	Psoas Muscle	Psoas
37	chr14:83108800-83109200	Active TSS	Right Ventricle	heart
38	chr14:83108800-83109200	Active TSS	Thymus	Thymus
39	chr14:83108800-83109400	Active TSS	Fetal Intestine Small	intestine
40	chr14:83108800-83109800	Active TSS	H1 Cell Line	embryonic stem cell
41	chr14:83109000-83109400	Active TSS	HUES64 Cell Line	embryonic stem cell
42	chr14:83109000-83109400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
43	chr14:83109000-83109400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr14:83109800-83112400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr14:83110200-83112400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr14:83110200-83112800	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr14:83110400-83110800	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr14:83110800-83111000	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr14:83111000-83112600	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr14:83112400-83113200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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