Variant report

Variant	nsv525630
Chromosome Location	chr15:79344324-79359310
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	ATF2	chr15:79352486-79352885	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr15:79352503-79352910	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr15:79352615-79352820	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr15:79346758-79346951	K562	blood:	n/a	n/a
5	CTBP2	chr15:79352464-79353309	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr15:79358420-79358570	GM12872	blood:	n/a	n/a
7	CTCF	chr15:79358320-79358470	HEK293	kidney:	n/a	n/a
8	CTCF	chr15:79344493-79344540	GM19239	blood:	n/a	chr15:79344509-79344527 chr15:79344510-79344526 chr15:79344504-79344525
9	CTCF	chr15:79358360-79358510	GM12864	blood:	n/a	n/a
10	CTCF	chr15:79344493-79344559	MCF-7	breast:	n/a	chr15:79344509-79344527 chr15:79344510-79344526 chr15:79344504-79344525
11	CTCF	chr15:79358380-79358530	GM12869	blood:	n/a	n/a
12	CTCF	chr15:79358406-79358478	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr15:79344454-79344589	H1-hESC	embryonic stem cell:	n/a	chr15:79344509-79344527 chr15:79344510-79344526 chr15:79344504-79344525
14	CTCF	chr15:79358580-79358730	GM12864	blood:	n/a	n/a
15	CTCF	chr15:79344420-79344570	SK-N-SH_RA	brain:	n/a	chr15:79344509-79344527 chr15:79344510-79344526 chr15:79344504-79344525
16	CTCF	chr15:79344440-79344590	HEK293	kidney:	n/a	chr15:79344509-79344527 chr15:79344510-79344526 chr15:79344504-79344525
17	CTCF	chr15:79344466-79344576	MCF-7	breast:	n/a	chr15:79344509-79344527 chr15:79344510-79344526 chr15:79344504-79344525
18	CTCF	chr15:79358412-79358486	GM12878	blood:	n/a	n/a
19	CTCF	chr15:79344490-79344494	MCF-7	breast:	n/a	n/a
20	CTCF	chr15:79344489-79344553	GM12891	blood:	n/a	chr15:79344509-79344527 chr15:79344510-79344526 chr15:79344504-79344525
21	CTCF	chr15:79358380-79358530	GM12873	blood:	n/a	n/a
22	CTCF	chr15:79358441-79358478	GM12892	blood:	n/a	n/a
23	CTCF	chr15:79358340-79358490	GM12864	blood:	n/a	n/a
24	CTCF	chr15:79358420-79358570	A549	lung:	n/a	n/a
25	CTCF	chr15:79358381-79358510	GM12878	blood:	n/a	n/a
26	CTCF	chr15:79344520-79344670	GM12865	blood:	n/a	n/a
27	CTCF	chr15:79344455-79344601	HepG2	liver:	n/a	chr15:79344509-79344527 chr15:79344510-79344526 chr15:79344504-79344525
28	CTCF	chr15:79358340-79358490	GM12878	blood:	n/a	n/a
29	CTCF	chr15:79358436-79358506	GM19238	blood:	n/a	n/a
30	CTCF	chr15:79358340-79358490	GM06990	blood:	n/a	n/a
31	CTCF	chr15:79358480-79358630	MCF-7	breast:	n/a	n/a
32	CTCF	chr15:79358420-79358570	GM12871	blood:	n/a	n/a
33	CTCF	chr15:79358460-79358610	GM12866	blood:	n/a	n/a
34	CTCF	chr15:79344540-79344690	GM12873	blood:	n/a	n/a
35	CTCF	chr15:79344496-79344540	MCF-7	breast:	n/a	chr15:79344509-79344527 chr15:79344510-79344526 chr15:79344504-79344525
36	CTCF	chr15:79344459-79344556	MCF-7	breast:	n/a	chr15:79344509-79344527 chr15:79344510-79344526 chr15:79344504-79344525
37	CTCF	chr15:79358340-79358490	GM12873	blood:	n/a	n/a
38	CTCF	chr15:79358420-79358570	GM12873	blood:	n/a	n/a
39	CTCF	chr15:79358400-79358550	GM12875	blood:	n/a	n/a
40	CTCF	chr15:79358360-79358510	HepG2	liver:	n/a	n/a
41	CTCF	chr15:79344481-79344562	MCF-7	breast:	n/a	chr15:79344509-79344527 chr15:79344510-79344526 chr15:79344504-79344525
42	CTCF	chr15:79358300-79358450	GM12874	blood:	n/a	n/a
43	CTCF	chr15:79358460-79358610	GM12872	blood:	n/a	n/a
44	CTCF	chr15:79344488-79344528	GM12892	blood:	n/a	chr15:79344509-79344527 chr15:79344510-79344526 chr15:79344504-79344525
45	CTCF	chr15:79358360-79358510	GM12874	blood:	n/a	n/a
46	CTCF	chr15:79358422-79358495	GM19240	blood:	n/a	n/a
47	CTCF	chr15:79344469-79344569	GM19238	blood:	n/a	chr15:79344509-79344527 chr15:79344510-79344526 chr15:79344504-79344525
48	E2F6	chr15:79346673-79347145	H1-hESC	embryonic stem cell:	n/a	n/a
49	EP300	chr15:79352419-79352960	H1-hESC	embryonic stem cell:	n/a	n/a
50	GTF2F1	chr15:79352554-79352751	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:79352412-79352462	Hepatocyte	liver:	n/a
2	chr15:79357037-79357087	ProgFib	skin:	n/a
3	chr15:79358128-79358178	AG09319	gingival:	n/a
4	chr15:79357037-79357087	HCT-116	colon:	n/a
5	chr15:79357160-79357210	MCF-7	breast:	n/a
6	chr15:79352412-79352462	HRE	kidney:	n/a
7	chr15:79352412-79352462	SK-N-SH	brain:	n/a
8	chr15:79352412-79352462	MCF10A-Er-Src	breast:	n/a
9	chr15:79352412-79352462	GM06990	blood:	n/a
10	chr15:79352412-79352462	T-47D	breast:	n/a
11	chr15:79352412-79352462	AG04450	lung:	fetal
12	chr15:79352412-79352462	Hela-S3	cervix:	n/a
13	chr15:79357160-79357210	HUVEC	blood vessel:	n/a
14	chr15:79352412-79352462	RPTEC	kidney:	n/a
15	chr15:79357037-79357087	Hela-S3	cervix:	n/a
16	chr15:79358128-79358178	HL-60	blood:	n/a
17	chr15:79352412-79352462	CMK	blood:	n/a
18	chr15:79358128-79358178	NHDF-neo	bronchial:	n/a
19	chr15:79358128-79358178	HEEpiC	esophagus:	n/a
20	chr15:79358128-79358178	HepG2	liver:	n/a
21	chr15:79352412-79352462	SKMC	muscle:	n/a
22	chr15:79357160-79357210	SK-N-SH_RA	brain:	n/a
23	chr15:79357037-79357087	IMR90	lung:	fetal
24	chr15:79358128-79358178	HNPCEpiC	eye:	n/a
25	chr15:79352412-79352462	LNCaP	prostate:	n/a
26	chr15:79357037-79357087	HRCEpiC	kidney:	n/a
27	chr15:79358128-79358178	A549	lung:	n/a
28	chr15:79352412-79352462	Jurkat	blood:	n/a
29	chr15:79358128-79358178	H1-hESC	embryonic stem cell:	embryo
30	chr15:79357037-79357087	K562	blood:	n/a
31	chr15:79352412-79352462	PANC-1	pancreas:	n/a
32	chr15:79357037-79357087	AoSMC	blood vessel:	n/a
33	chr15:79357160-79357210	HRCEpiC	kidney:	n/a
34	chr15:79357037-79357087	MCF10A-Er-Src	breast:	n/a
35	chr15:79358128-79358178	GM12878	blood:	n/a
36	chr15:79352412-79352462	ProgFib	skin:	n/a
37	chr15:79352412-79352462	HCT-116	colon:	n/a
38	chr15:79357160-79357210	HEEpiC	esophagus:	n/a
39	chr15:79357160-79357210	CMK	blood:	n/a
40	chr15:79358128-79358178	MCF-7	breast:	n/a
41	chr15:79358128-79358178	NHBE	bronchial:	n/a
42	chr15:79358128-79358178	SK-N-MC	brain:	n/a
43	chr15:79357160-79357210	BJ	skin:	n/a
44	chr15:79357160-79357210	AG10803	skin:	n/a
45	chr15:79352412-79352462	HepG2	liver:	n/a
46	chr15:79357160-79357210	HRE	kidney:	n/a
47	chr15:79357037-79357087	AG04449	skin:	fetal
48	chr15:79357160-79357210	AG09319	gingival:	n/a
49	chr15:79357037-79357087	ovcar-3	ovarian:	n/a
50	chr15:79357037-79357087	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:79353540..79355463-chr15:79584936..79587312,2	MCF-7	breast:
2	chr15:79343404..79345665-chr15:79347636..79349746,2	MCF-7	breast:
3	chr15:79343404..79345665-chr15:79347636..79349746,2	MCF-7	breast:
4	chr15:79351623..79352456-chr9:116148392..116149161,2	MCF-7	breast:
5	chr15:79338009..79340496-chr15:79344348..79345956,2	MCF-7	breast:
6	chr15:79347249..79349881-chr15:79351667..79353253,2	MCF-7	breast:
7	chr15:79347249..79349881-chr15:79351667..79353253,2	MCF-7	breast:
8	chr15:79358143..79360952-chr15:79361346..79363073,2	K562	blood:
9	chr15:79317932..79319817-chr15:79350571..79352608,2	K562	blood:

Variant related genes	Relation type
RASGRF1	TF binding region
RASGRF1	CpG island
ENSG00000235711	chromatin interactions

Extended variants
information (count: 582 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:582 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12440502	chr15:79344324-79344325	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs539884851	chr15:79344332-79344333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544651290	chr15:79344337-79344338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183667034	chr15:79344376-79344377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs77773016	chr15:79344377-79344378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187128630	chr15:79344381-79344382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561106988	chr15:79344391-79344392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190614407	chr15:79344408-79344409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs11072824	chr15:79344416-79344417	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs73477322	chr15:79344470-79344471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532550003	chr15:79344472-79344473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs369121785	chr15:79344483-79344484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568915034	chr15:79344547-79344548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182764635	chr15:79344557-79344558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568577075	chr15:79344558-79344559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs115828459	chr15:79344564-79344565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs373967253	chr15:79344709-79344710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs377380864	chr15:79344712-79344713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568598696	chr15:79344745-79344746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537250182	chr15:79344746-79344747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs116174159	chr15:79344821-79344822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs139061372	chr15:79344825-79344826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs187242597	chr15:79344874-79344875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs558156535	chr15:79344929-79344930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149532607	chr15:79344935-79344936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540692746	chr15:79345032-79345033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144177025	chr15:79345050-79345051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539407850	chr15:79345063-79345064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs77277610	chr15:79345110-79345111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs146547434	chr15:79345136-79345137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531107106	chr15:79345161-79345162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563590171	chr15:79345178-79345179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs143395473	chr15:79345196-79345197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs550799716	chr15:79345221-79345222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146565666	chr15:79345280-79345281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs190143485	chr15:79345293-79345294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs528503552	chr15:79345348-79345349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs376192463	chr15:79345363-79345364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs112090572	chr15:79345382-79345383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs568507948	chr15:79345419-79345420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs370575230	chr15:79345436-79345437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372670189	chr15:79345467-79345468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570964924	chr15:79345473-79345474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187469462	chr15:79345474-79345475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs550926216	chr15:79345475-79345476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs570785010	chr15:79345476-79345477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539714121	chr15:79345482-79345483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539936715	chr15:79345503-79345504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs193295097	chr15:79345555-79345556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553430475	chr15:79345556-79345557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:134 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:79338600-79346400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr15:79342200-79348400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:79342200-79349400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr15:79342800-79345200	Enhancers	Brain Angular Gyrus	brain
5	chr15:79343000-79344600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr15:79343000-79345000	Enhancers	Brain Hippocampus Middle	brain
7	chr15:79343000-79345000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
8	chr15:79343000-79345200	Enhancers	Brain Cingulate Gyrus	brain
9	chr15:79343000-79345200	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr15:79343000-79347200	Enhancers	Brain Substantia Nigra	brain
11	chr15:79343400-79344800	Enhancers	Fetal Brain Female	brain
12	chr15:79343600-79344800	Enhancers	Brain Anterior Caudate	brain
13	chr15:79344200-79345000	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr15:79344200-79345000	Enhancers	Gastric	stomach
15	chr15:79344200-79345000	Enhancers	Lung	lung
16	chr15:79344200-79345200	Enhancers	Right Atrium	heart
17	chr15:79344400-79344600	Enhancers	Brain Germinal Matrix	brain
18	chr15:79344800-79346000	Weak transcription	Brain Germinal Matrix	brain
19	chr15:79344800-79356600	Weak transcription	Brain Anterior Caudate	brain
20	chr15:79345000-79346200	Weak transcription	Brain Hippocampus Middle	brain
21	chr15:79345000-79348600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr15:79345200-79346000	Weak transcription	Brain Angular Gyrus	brain
23	chr15:79345200-79346400	Weak transcription	Brain Cingulate Gyrus	brain
24	chr15:79345200-79346400	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr15:79345200-79350200	Weak transcription	Right Atrium	heart
26	chr15:79346000-79346200	Enhancers	Brain Angular Gyrus	brain
27	chr15:79346000-79346600	Enhancers	Brain Germinal Matrix	brain
28	chr15:79346200-79346600	Genic enhancers	Brain Angular Gyrus	brain
29	chr15:79346200-79346600	Enhancers	Brain Hippocampus Middle	brain
30	chr15:79346400-79346600	Enhancers	Brain Cingulate Gyrus	brain
31	chr15:79346400-79347400	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr15:79346400-79349800	Strong transcription	Pancreatic Islets	Pancreatic Islet
33	chr15:79346600-79347400	Genic enhancers	Brain Cingulate Gyrus	brain
34	chr15:79346600-79349800	Strong transcription	Brain Angular Gyrus	brain
35	chr15:79346600-79355600	Weak transcription	Brain Hippocampus Middle	brain
36	chr15:79347200-79351800	Weak transcription	Brain Substantia Nigra	brain
37	chr15:79347400-79348200	Weak transcription	Brain Cingulate Gyrus	brain
38	chr15:79347400-79348200	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr15:79348200-79348400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr15:79348200-79350400	Strong transcription	Brain Cingulate Gyrus	brain
41	chr15:79348200-79350800	Strong transcription	Brain Inferior Temporal Lobe	brain
42	chr15:79348400-79349200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr15:79348600-79350800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr15:79349200-79349600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr15:79349400-79349600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr15:79349800-79356600	Weak transcription	Brain Angular Gyrus	brain
47	chr15:79349800-79361000	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr15:79350400-79351800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
49	chr15:79350400-79353200	Weak transcription	Brain Cingulate Gyrus	brain
50	chr15:79350600-79351000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell

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