Variant report

Variant	nsv974713
Chromosome Location	chr15:78945824-78996783
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:247)
CpG islands
(count:427)
Chromatin interactive
region (count:16)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:247 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:78960071-78960144	HepG2	liver:	n/a	n/a
2	ATF2	chr15:78968759-78969247	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr15:78964662-78964945	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr15:78958455-78958708	GM12878	blood:	n/a	n/a
5	BHLHE40	chr15:78988350-78988562	K562	blood:	n/a	n/a
6	BRCA1	chr15:78956789-78956836	GM12878	blood:	n/a	n/a
7	CEBPB	chr15:78971172-78971449	A549	lung:	n/a	chr15:78971284-78971301
8	CEBPB	chr15:78971173-78971447	HepG2	liver:	n/a	chr15:78971284-78971301
9	CEBPB	chr15:78971178-78971448	Hela-S3	cervix:	n/a	chr15:78971284-78971301
10	CEBPD	chr15:78988310-78988599	K562	blood:	n/a	n/a
11	CTCF	chr15:78987000-78987150	GM12865	blood:	n/a	n/a
12	CTCF	chr15:78988311-78988409	MCF-7	breast:	n/a	chr15:78988352-78988370
13	CTCF	chr15:78988185-78988555	K562	blood:	n/a	chr15:78988352-78988370
14	CTCF	chr15:78988140-78988290	HCM	heart:	n/a	n/a
15	CTCF	chr15:78988280-78988430	GM12873	blood:	n/a	chr15:78988352-78988370
16	CTCF	chr15:78985720-78985870	A549	lung:	n/a	n/a
17	CTCF	chr15:78988300-78988450	HepG2	liver:	n/a	chr15:78988352-78988370
18	CTCF	chr15:78956880-78957030	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr15:78996180-78996252	GM12892	blood:	n/a	n/a
20	CTCF	chr15:78988180-78988330	HRPEpiC	eye:	n/a	n/a
21	CTCF	chr15:78996184-78996203	GM12891	blood:	n/a	n/a
22	CTCF	chr15:78988273-78988458	K562	blood:	n/a	chr15:78988352-78988370
23	CTCF	chr15:78977640-78977790	GM12871	blood:	n/a	n/a
24	CTCF	chr15:78988286-78988435	H1-hESC	embryonic stem cell:	n/a	chr15:78988352-78988370
25	CTCF	chr15:78988321-78988410	Pancreas_OC	pancreas:	n/a	chr15:78988352-78988370
26	CTCF	chr15:78988260-78988410	GM12871	blood:	n/a	chr15:78988352-78988370
27	CTCF	chr15:78988200-78988350	GM12865	blood:	n/a	n/a
28	CTCF	chr15:78988240-78988602	K562	blood:	n/a	chr15:78988352-78988370
29	CTCF	chr15:78988298-78988426	Gliobla	brain:	n/a	chr15:78988352-78988370
30	CTCF	chr15:78988209-78988482	K562	blood:	n/a	chr15:78988352-78988370
31	CTCF	chr15:78988319-78988422	SK-N-SH_RA	brain:	n/a	chr15:78988352-78988370
32	CTCF	chr15:78988425-78988428	LNCaP	prostate:	n/a	n/a
33	CTCF	chr15:78988260-78988410	HPAF	blood vessel:	n/a	chr15:78988352-78988370
34	CTCF	chr15:78964340-78964490	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr15:78988358-78988427	GM12878	blood:	n/a	n/a
36	CTCF	chr15:78988220-78988370	SK-N-SH_RA	brain:	n/a	chr15:78988352-78988370
37	CTCF	chr15:78988200-78988350	HMEC	breast:	n/a	n/a
38	CTCF	chr15:78988280-78988430	SAEC	small airway:	n/a	chr15:78988352-78988370
39	CTCF	chr15:78963840-78963990	BE2_C	brain:	n/a	chr15:78963950-78963958
40	CTCF	chr15:78988280-78988426	MCF-7	breast:	n/a	chr15:78988352-78988370
41	CTCF	chr15:78988292-78988442	MCF-7	breast:	n/a	chr15:78988352-78988370
42	CTCF	chr15:78988280-78988430	K562	blood:	n/a	chr15:78988352-78988370
43	CTCF	chr15:78988300-78988450	NHEK	skin:	n/a	chr15:78988352-78988370
44	CTCF	chr15:78988280-78988430	HBMEC	blood vessel:	n/a	chr15:78988352-78988370
45	CTCF	chr15:78987180-78987330	GM12869	blood:	n/a	n/a
46	CTCF	chr15:78995760-78995910	NHEK	skin:	n/a	n/a
47	CTCF	chr15:78988344-78988487	Spleen_OC	spleen:	n/a	chr15:78988352-78988370
48	CTCF	chr15:78988300-78988450	SK-N-SH_RA	brain:	n/a	chr15:78988352-78988370
49	CTCF	chr15:78988260-78988410	WERI-Rb-1	eye:	n/a	chr15:78988352-78988370
50	CTCF	chr15:78988292-78988427	MCF-7	breast:	n/a	chr15:78988352-78988370

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78953682-78953732	SKMC	muscle:	n/a
2	chr15:78968879-78968929	HAEpiC	amniotic membrane:	n/a
3	chr15:78953682-78953732	BJ	skin:	n/a
4	chr15:78978136-78978186	HPAEpiC	pulmonary alveolar:	n/a
5	chr15:78953907-78953957	GM19239	blood:	n/a
6	chr15:78953907-78953957	NHBE	bronchial:	n/a
7	chr15:78953473-78953523	HPAEpiC	pulmonary alveolar:	n/a
8	chr15:78953473-78953523	LNCaP	prostate:	n/a
9	chr15:78968879-78968929	IMR90	lung:	fetal
10	chr15:78953907-78953957	HRPEpiC	eye:	n/a
11	chr15:78953907-78953957	NT2-D1	testis:	n/a
12	chr15:78984179-78984229	HMEC	breast:	n/a
13	chr15:78953473-78953523	MCF10A-Er-Src	breast:	n/a
14	chr15:78953028-78953078	AG04449	skin:	fetal
15	chr15:78953682-78953732	NB4	blood:	n/a
16	chr15:78968879-78968929	HRPEpiC	eye:	n/a
17	chr15:78978136-78978186	HUVEC	blood vessel:	n/a
18	chr15:78978136-78978186	SK-N-SH_RA	brain:	n/a
19	chr15:78953907-78953957	HCF	heart:	n/a
20	chr15:78953473-78953523	A549	lung:	n/a
21	chr15:78953473-78953523	BE2_C	brain:	n/a
22	chr15:78978136-78978186	NHBE	bronchial:	n/a
23	chr15:78953682-78953732	H1-hESC	embryonic stem cell:	embryo
24	chr15:78968879-78968929	GM06990	blood:	n/a
25	chr15:78953907-78953957	K562	blood:	n/a
26	chr15:78968879-78968929	A549	lung:	n/a
27	chr15:78953028-78953078	Jurkat	blood:	n/a
28	chr15:78953473-78953523	AG10803	skin:	n/a
29	chr15:78953473-78953523	HRE	kidney:	n/a
30	chr15:78953473-78953523	H1-hESC	embryonic stem cell:	embryo
31	chr15:78953028-78953078	AG10803	skin:	n/a
32	chr15:78953682-78953732	HNPCEpiC	eye:	n/a
33	chr15:78953682-78953732	HRE	kidney:	n/a
34	chr15:78968879-78968929	AG04450	lung:	fetal
35	chr15:78968879-78968929	HRE	kidney:	n/a
36	chr15:78953907-78953957	HMEC	breast:	n/a
37	chr15:78968879-78968929	HNPCEpiC	eye:	n/a
38	chr15:78953682-78953732	HUVEC	blood vessel:	n/a
39	chr15:78953682-78953732	GM12892	blood:	n/a
40	chr15:78984179-78984229	PFSK-1	brain:	n/a
41	chr15:78968879-78968929	AG04449	skin:	fetal
42	chr15:78978136-78978186	ECC-1	luminal epithelium:	n/a
43	chr15:78978136-78978186	HEK293	kidney:	embryo
44	chr15:78953028-78953078	ECC-1	luminal epithelium:	n/a
45	chr15:78953907-78953957	GM12891	blood:	n/a
46	chr15:78968879-78968929	HCPEpiC	choroid plexus:	n/a
47	chr15:78953028-78953078	HEEpiC	esophagus:	n/a
48	chr15:78953907-78953957	LNCaP	prostate:	n/a
49	chr15:78978136-78978186	HL-60	blood:	n/a
50	chr15:78968879-78968929	AoSMC	blood vessel:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:78970161..78972429-chr15:78973595..78976262,2	K562	blood:
2	chr15:78977969..78980271-chr15:78982460..78985285,2	K562	blood:
3	chr15:78977969..78980271-chr15:78982460..78985285,2	K562	blood:
4	chr15:78983381..78985912-chr15:78992265..78995147,2	MCF-7	breast:
5	chr15:78923736..78925792-chr15:78976356..78977930,2	K562	blood:
6	chr15:78970161..78972429-chr15:78973595..78976262,2	K562	blood:
7	chr15:78983381..78985912-chr15:78992265..78995147,2	MCF-7	breast:
8	chr15:78942804..78945237-chr15:78946010..78948763,2	K562	blood:
9	chr15:78963617..78966292-chr15:78967103..78969117,2	K562	blood:
10	chr15:78963617..78966292-chr15:78967103..78969117,2	K562	blood:
11	chr15:78963944..78966069-chr3:64562152..64564273,2	MCF-7	breast:
12	chr15:78949342..78952900-chr15:78954875..78958470,3	K562	blood:
13	chr15:78954699..78956761-chr15:78960966..78963613,2	MCF-7	breast:
14	chr15:78954699..78956761-chr15:78960966..78963613,2	MCF-7	breast:
15	chr15:78983812..78985475-chr15:79007336..79009142,2	MCF-7	breast:
16	chr15:78912983..78915101-chr15:78972644..78975199,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAMTS7-1	chr15:78979260-78979741	ENSG00000259329.1
2	lnc-CHRNA5-3	chr15:78996190-78996226	NONHSAT047586
3	lnc-CHRNA5-3	chr15:78996118-78996314	NONHSAT047592
4	lnc-CHRNA5-3	chr15:78952986-78953211	NONHSAT047586
5	lnc-CHRNA3-4	chr15:78953389-78953918	NONHSAT047587
6	lnc-ADAMTS7-1	chr15:78984920-78985236	ENSG00000259329.1
7	lnc-CHRNA5-3	chr15:78985024-78985188	NONHSAT047586
8	lnc-CHRNA5-3	chr15:78953737-78953876	NONHSAT047586

No data

Variant related genes	Relation type
ENSG00000261303	TF binding region
RPL18P11	TF binding region
CHRNB4	TF binding region
ENSG00000261303	CpG island
RPL18P11	CpG island
CHRNB4	CpG island
ENSG00000080644	chromatin interactions
ENSG00000117971	chromatin interactions

Extended variants
information (count: 1889 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1889 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183841249	chr15:78945829-78945830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs554104390	chr15:78945848-78945849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574011829	chr15:78945864-78945865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538125816	chr15:78945934-78945935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35238224	chr15:78945981-78945982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs397853825	chr15:78945982-78945983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145990613	chr15:78946007-78946008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186548436	chr15:78946023-78946024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs115572060	chr15:78946034-78946035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191463484	chr15:78946052-78946053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs56778876	chr15:78946110-78946111	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs572565602	chr15:78946130-78946131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182552178	chr15:78946144-78946145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561246490	chr15:78946146-78946147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs186878189	chr15:78946183-78946184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191547822	chr15:78946201-78946202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182249003	chr15:78946239-78946240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs118092991	chr15:78946248-78946249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547270431	chr15:78946263-78946264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565477648	chr15:78946278-78946279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536015979	chr15:78946312-78946313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529724492	chr15:78946364-78946365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139630158	chr15:78946367-78946368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569330141	chr15:78946390-78946391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536607054	chr15:78946428-78946429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs79491334	chr15:78946441-78946442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554405966	chr15:78946466-78946467	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs77883125	chr15:78946511-78946512	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554393581	chr15:78946549-78946550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572602818	chr15:78946617-78946618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12594247	chr15:78946633-78946634	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs189226945	chr15:78946662-78946663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144247470	chr15:78946715-78946716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543405137	chr15:78946716-78946717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538263152	chr15:78946721-78946722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs193004317	chr15:78946748-78946749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541252926	chr15:78946770-78946771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34622606	chr15:78946784-78946785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370247989	chr15:78946791-78946792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375966592	chr15:78946819-78946820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs117214547	chr15:78946820-78946821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35608162	chr15:78946826-78946827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1021070	chr15:78946863-78946864	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs569368094	chr15:78946905-78946906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530527812	chr15:78946935-78946936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs77597850	chr15:78946942-78946943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185314520	chr15:78946947-78946948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116959742	chr15:78947058-78947059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554479365	chr15:78947156-78947157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533554997	chr15:78947166-78947167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:402 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78933800-78960200	Weak transcription	Right Atrium	heart
2	chr15:78946400-78946800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
3	chr15:78953800-78955000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr15:78954000-78954800	Enhancers	HepG2	liver
5	chr15:78954200-78954600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr15:78954200-78954600	Enhancers	Spleen	Spleen
7	chr15:78954400-78954600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr15:78954600-78959200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr15:78956200-78956400	Enhancers	GM12878-XiMat	blood
10	chr15:78956800-78957000	Enhancers	Fetal Kidney	kidney
11	chr15:78957000-78964200	Weak transcription	Fetal Kidney	kidney
12	chr15:78958200-78959200	Enhancers	GM12878-XiMat	blood
13	chr15:78959200-78959400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr15:78959200-78961000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr15:78959800-78960000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
16	chr15:78959800-78960600	Enhancers	Left Ventricle	heart
17	chr15:78959800-78960600	Enhancers	Right Ventricle	heart
18	chr15:78959800-78960600	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr15:78959800-78960800	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr15:78959800-78960800	Enhancers	HepG2	liver
21	chr15:78960000-78960200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
22	chr15:78960200-78960400	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr15:78960200-78960400	Enhancers	Right Atrium	heart
24	chr15:78960400-78960800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
25	chr15:78960400-78960800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
26	chr15:78960600-78964200	Weak transcription	Left Ventricle	heart
27	chr15:78960600-78964200	Weak transcription	Right Ventricle	heart
28	chr15:78960800-78961000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr15:78960800-78961800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr15:78960800-78963600	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr15:78960800-78964200	Weak transcription	HepG2	liver
32	chr15:78961000-78963600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr15:78961000-78964000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr15:78961400-78961600	Enhancers	H9 Cell Line	embryonic stem cell
35	chr15:78961400-78961800	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr15:78961400-78962000	Enhancers	Fetal Stomach	stomach
37	chr15:78961400-78962200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
38	chr15:78961400-78962200	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr15:78961400-78962400	Enhancers	H1 Cell Line	embryonic stem cell
40	chr15:78961400-78962400	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr15:78961600-78961800	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr15:78961600-78961800	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr15:78961600-78964800	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr15:78961800-78962000	Enhancers	Placenta	Placenta
45	chr15:78961800-78963600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr15:78961800-78964200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr15:78962000-78963600	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr15:78962000-78964000	Weak transcription	Fetal Stomach	stomach
49	chr15:78962200-78963600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr15:78962400-78963400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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