Variant report

Variant	nsv904429
Chromosome Location	chr15:78160362-78251431
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3087)
CpG islands
(count:1468)
Chromatin interactive
region (count:25)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3087 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:78237679-78237763	K562	blood:	n/a	n/a
2	ARID3A	chr15:78236893-78236910	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:78235026-78235383	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:78162883-78163100	HepG2	liver:	n/a	n/a
5	ATF1	chr15:78219190-78219467	K562	blood:	n/a	n/a
6	ATF3	chr15:78236808-78236989	K562	blood:	n/a	n/a
7	ATF3	chr15:78246365-78246569	K562	blood:	n/a	n/a
8	BACH1	chr15:78191284-78191344	K562	blood:	n/a	n/a
9	BATF	chr15:78200510-78200771	GM12878	blood:	n/a	n/a
10	BATF	chr15:78240702-78240880	GM12878	blood:	n/a	n/a
11	BATF	chr15:78246140-78246599	GM12878	blood:	n/a	n/a
12	BATF	chr15:78202770-78203254	GM12878	blood:	n/a	n/a
13	BATF	chr15:78246086-78246649	GM12878	blood:	n/a	n/a
14	BCL11A	chr15:78246237-78246453	GM12878	blood:	n/a	n/a
15	BCL11A	chr15:78183650-78183946	GM12878	blood:	n/a	n/a
16	BCL11A	chr15:78202965-78203220	GM12878	blood:	n/a	chr15:78202981-78202994
17	BCL11A	chr15:78236927-78237145	GM12878	blood:	n/a	n/a
18	BCL11A	chr15:78181243-78181441	GM12878	blood:	n/a	chr15:78181308-78181321
19	BCL11A	chr15:78246175-78246575	GM12878	blood:	n/a	n/a
20	BCL3	chr15:78177756-78178421	GM12878	blood:	n/a	n/a
21	BCL3	chr15:78191128-78191516	GM12878	blood:	n/a	n/a
22	BCL3	chr15:78177816-78178379	GM12878	blood:	n/a	n/a
23	BCL3	chr15:78191134-78191391	GM12878	blood:	n/a	n/a
24	BCL3	chr15:78177167-78177695	GM12878	blood:	n/a	chr15:78177500-78177509 chr15:78177265-78177274
25	BCL3	chr15:78177235-78177691	GM12878	blood:	n/a	chr15:78177500-78177509 chr15:78177265-78177274
26	BHLHE40	chr15:78200229-78200546	K562	blood:	n/a	n/a
27	BHLHE40	chr15:78236781-78237088	HepG2	liver:	n/a	n/a
28	BHLHE40	chr15:78162937-78162982	GM12878	blood:	n/a	n/a
29	BHLHE40	chr15:78200363-78200447	GM12878	blood:	n/a	n/a
30	BHLHE40	chr15:78236789-78237064	GM12878	blood:	n/a	n/a
31	BHLHE40	chr15:78192717-78192924	K562	blood:	n/a	n/a
32	BHLHE40	chr15:78183229-78183978	GM12878	blood:	n/a	n/a
33	BHLHE40	chr15:78191369-78191376	K562	blood:	n/a	n/a
34	BHLHE40	chr15:78203005-78203198	GM12878	blood:	n/a	n/a
35	BHLHE40	chr15:78192723-78193286	GM12878	blood:	n/a	n/a
36	BHLHE40	chr15:78167567-78167705	GM12878	blood:	n/a	n/a
37	BHLHE40	chr15:78197822-78197825	K562	blood:	n/a	n/a
38	BHLHE40	chr15:78162833-78163083	K562	blood:	n/a	n/a
39	BHLHE40	chr15:78181314-78181673	GM12878	blood:	n/a	n/a
40	BHLHE40	chr15:78202964-78203186	K562	blood:	n/a	n/a
41	BHLHE40	chr15:78161395-78161648	GM12878	blood:	n/a	n/a
42	BHLHE40	chr15:78177249-78177916	GM12878	blood:	n/a	n/a
43	BHLHE40	chr15:78190603-78190942	K562	blood:	n/a	chr15:78190757-78190766 chr15:78190757-78190766 chr15:78190758-78190767
44	BHLHE40	chr15:78176969-78177063	K562	blood:	n/a	n/a
45	BHLHE40	chr15:78195387-78195410	GM12878	blood:	n/a	n/a
46	BHLHE40	chr15:78236789-78237097	K562	blood:	n/a	n/a
47	BRCA1	chr15:78200667-78200670	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr15:78203014-78203173	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr15:78177537-78177695	GM12878	blood:	n/a	n/a
50	CBX3	chr15:78200531-78200865	K562	blood:	n/a	n/a

(count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78189695-78189745	HAEpiC	amniotic membrane:	n/a
2	chr15:78189695-78189745	IMR90	lung:	fetal
3	chr15:78236860-78236910	AoSMC	blood vessel:	n/a
4	chr15:78219273-78219323	GM06990	blood:	n/a
5	chr15:78189695-78189745	HAEpiC	amniotic membrane:	n/a
6	chr15:78189695-78189745	IMR90	lung:	fetal
7	chr15:78236860-78236910	AoSMC	blood vessel:	n/a
8	chr15:78219273-78219323	GM06990	blood:	n/a
9	chr15:78190123-78190173	ProgFib	skin:	n/a
10	chr15:78209119-78209169	GM12878	blood:	n/a
11	chr15:78194488-78194538	SKMC	muscle:	n/a
12	chr15:78238416-78238466	BJ	skin:	n/a
13	chr15:78189695-78189745	NB4	blood:	n/a
14	chr15:78219748-78219798	GM12892	blood:	n/a
15	chr15:78208251-78208301	AG09309	skin:	n/a
16	chr15:78236860-78236910	IMR90	lung:	fetal
17	chr15:78190123-78190173	PrEC	prostate:	n/a
18	chr15:78240223-78240273	T-47D	breast:	n/a
19	chr15:78233786-78233836	HPAEpiC	pulmonary alveolar:	n/a
20	chr15:78191302-78191352	AG04450	lung:	fetal
21	chr15:78235484-78235534	HAEpiC	amniotic membrane:	n/a
22	chr15:78191345-78191395	SK-N-MC	brain:	n/a
23	chr15:78189752-78189802	ECC-1	luminal epithelium:	n/a
24	chr15:78186622-78186672	ProgFib	skin:	n/a
25	chr15:78236707-78236757	GM12892	blood:	n/a
26	chr15:78219273-78219323	RPTEC	kidney:	n/a
27	chr15:78240223-78240273	ovcar-3	ovarian:	n/a
28	chr15:78186622-78186672	HCF	heart:	n/a
29	chr15:78189752-78189802	HAEpiC	amniotic membrane:	n/a
30	chr15:78194488-78194538	BJ	skin:	n/a
31	chr15:78189752-78189802	LNCaP	prostate:	n/a
32	chr15:78189695-78189745	MCF10A-Er-Src	breast:	n/a
33	chr15:78236860-78236910	HMEC	breast:	n/a
34	chr15:78196623-78196673	K562	blood:	n/a
35	chr15:78200484-78200534	ProgFib	skin:	n/a
36	chr15:78219748-78219798	HEEpiC	esophagus:	n/a
37	chr15:78189695-78189745	ProgFib	skin:	n/a
38	chr15:78191302-78191352	HEEpiC	esophagus:	n/a
39	chr15:78240223-78240273	MCF10A-Er-Src	breast:	n/a
40	chr15:78189695-78189745	NHBE	bronchial:	n/a
41	chr15:78235484-78235534	PANC-1	pancreas:	n/a
42	chr15:78238416-78238466	AG10803	skin:	n/a
43	chr15:78238416-78238466	HCT-116	colon:	n/a
44	chr15:78191345-78191395	Jurkat	blood:	n/a
45	chr15:78238416-78238466	SK-N-SH_RA	brain:	n/a
46	chr15:78189695-78189745	PANC-1	pancreas:	n/a
47	chr15:78191345-78191395	GM12891	blood:	n/a
48	chr15:78219423-78219473	AG04449	skin:	fetal
49	chr15:78238416-78238466	H1-hESC	embryonic stem cell:	embryo
50	chr15:78196623-78196673	HEK293	kidney:	embryo

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:75978451..75979139-chr15:78192424..78193254,5	MCF-7	breast:
2	chr15:78251411..78252367-chr15:78280153..78280696,2	MCF-7	breast:
3	chr15:78162688..78164962-chr15:78166571..78168544,2	K562	blood:
4	chr15:78194874..78195656-chr15:78400670..78401266,2	MCF-7	breast:
5	chr15:77942627..77943302-chr15:78167255..78168112,2	MCF-7	breast:
6	chr15:78200418..78201162-chr15:78910453..78911204,2	K562	blood:
7	chr15:78170552..78173513-chr15:78177098..78179231,2	K562	blood:
8	chr15:77925526..77926907-chr15:78167143..78168054,6	MCF-7	breast:
9	chr15:77925519..77926294-chr15:78162494..78163468,3	MCF-7	breast:
10	chr15:75975803..75976315-chr15:78195454..78196010,2	K562	blood:
11	chr15:78151280..78153244-chr15:78194302..78196153,2	MCF-7	breast:
12	chr15:77925576..77926405-chr15:78167119..78167924,3	K562	blood:
13	chr15:78115470..78116424-chr15:78167241..78167877,2	MCF-7	breast:
14	chr15:78162688..78164962-chr15:78166571..78168544,2	K562	blood:
15	chr15:78251353..78252448-chr15:78400281..78401311,8	MCF-7	breast:
16	chr15:78170552..78173513-chr15:78177098..78179231,2	K562	blood:
17	chr15:78236783..78237478-chrX:151999319..151999901,2	NB4	blood:
18	chr15:77925583..77927500-chr15:78167130..78168054,7	MCF-7	breast:
19	chr15:77835482..77836422-chr15:78167231..78168063,2	K562	blood:
20	chr15:77951644..77952520-chr15:78167212..78167992,3	MCF-7	breast:
21	chr15:78232364..78235120-chr15:78235300..78238762,3	K562	blood:
22	chr15:75978476..75979174-chr15:78192448..78193224,3	MCF-7	breast:
23	chr15:78232364..78235120-chr15:78235300..78238762,3	K562	blood:
24	chr15:78200661..78201180-chr15:79032859..79033389,2	MCF-7	breast:
25	chr15:78251300..78252464-chr15:78292151..78292856,3	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TBC1D2B-5	chr15:78209065-78209324	NONHSAT047472
2	lnc-TBC1D2B-1	chr15:78246417-78246686	ENSG00000261403.1
3	lnc-SH2D7-4	chr15:78208864-78208974	ENSG00000261244.1
4	lnc-SH2D7-4	chr15:78214120-78214361	ENSG00000261244.1

No data

Variant related genes	Relation type
CSPG4P13	TF binding region
ENSG00000261244	TF binding region
RN7SL214P	TF binding region
ENSG00000260776	TF binding region
ENSG00000214646	TF binding region
CSPG4P13	CpG island
ENSG00000261244	CpG island
RN7SL214P	CpG island
ENSG00000260776	CpG island
ENSG00000214646	CpG island
ENSG00000169783	chromatin interactions
ENSG00000261143	chromatin interactions
ENSG00000147400	chromatin interactions
ENSG00000214646	chromatin interactions
ENSG00000147383	chromatin interactions
ENSG00000259281	chromatin interactions

Extended variants
information (count: 4494 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:4494 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3901402	chr15:78160362-78160363	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575357319	chr15:78160372-78160373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs142054493	chr15:78160419-78160420	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs28522551	chr15:78160453-78160454	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs564487381	chr15:78160457-78160458	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs534565147	chr15:78160459-78160460	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs528141552	chr15:78160487-78160488	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs547992778	chr15:78160494-78160495	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs559551468	chr15:78160499-78160500	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs537430282	chr15:78160500-78160501	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs370343487	chr15:78160541-78160542	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs530217334	chr15:78160547-78160548	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs28494785	chr15:78160591-78160592	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs570014162	chr15:78160658-78160659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537459684	chr15:78160673-78160674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552251170	chr15:78160702-78160703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs28405381	chr15:78160711-78160712	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs534832702	chr15:78160732-78160733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112670004	chr15:78160736-78160737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553487566	chr15:78160777-78160778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs574725632	chr15:78160778-78160779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370116354	chr15:78160802-78160803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374684639	chr15:78160834-78160835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184261761	chr15:78160891-78160892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557295941	chr15:78160927-78160928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs75066885	chr15:78160935-78160936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs117757011	chr15:78160956-78160957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372601131	chr15:78160983-78160984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs367884282	chr15:78161003-78161004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs111572696	chr15:78161004-78161005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543007029	chr15:78161049-78161050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545800026	chr15:78161057-78161058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557441865	chr15:78161073-78161074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572776449	chr15:78161106-78161107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539976053	chr15:78161146-78161147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555023888	chr15:78161193-78161194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371169899	chr15:78161216-78161217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs75856043	chr15:78161265-78161266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs79178608	chr15:78161288-78161289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561440304	chr15:78161296-78161297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs34320251	chr15:78161314-78161315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs35713688	chr15:78161320-78161321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10152492	chr15:78161374-78161375	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs377088143	chr15:78161388-78161389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs541975658	chr15:78161418-78161419	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs10152449	chr15:78161430-78161431	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs531081716	chr15:78161457-78161458	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs565275875	chr15:78161476-78161477	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs552810738	chr15:78161533-78161534	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs570790473	chr15:78161536-78161537	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Breast cancer	17133270	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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1196 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78152400-78161400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr15:78155400-78161400	Weak transcription	HSMM	muscle
3	chr15:78155800-78163000	Weak transcription	Fetal Intestine Small	intestine
4	chr15:78157000-78161400	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr15:78157600-78162400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr15:78157800-78161400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr15:78159000-78160400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr15:78159800-78161200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr15:78160200-78160400	Enhancers	Pancreas	Pancrea
10	chr15:78160400-78160600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
11	chr15:78160400-78161400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr15:78160400-78162800	Weak transcription	Pancreas	Pancrea
13	chr15:78161200-78162600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr15:78161200-78163000	Enhancers	Hela-S3	cervix
15	chr15:78161400-78162000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr15:78161400-78162000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr15:78161400-78162000	Enhancers	Placenta	Placenta
18	chr15:78161400-78162200	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr15:78161400-78162200	Enhancers	Muscle Satellite Cultured Cells	--
20	chr15:78161400-78162200	Enhancers	HSMMtube	muscle
21	chr15:78161400-78162400	Enhancers	HMEC	breast
22	chr15:78161400-78162800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr15:78161400-78162800	Enhancers	HUVEC	blood vessel
24	chr15:78161400-78163200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr15:78161400-78163200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr15:78161400-78163200	Enhancers	HSMM	muscle
27	chr15:78161400-78163400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr15:78161600-78162200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr15:78161600-78162200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
30	chr15:78161600-78162200	Enhancers	NH-A	brain
31	chr15:78161800-78162000	Enhancers	A549	lung
32	chr15:78161800-78162200	Enhancers	Osteobl	bone
33	chr15:78162000-78162200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr15:78162000-78162200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
35	chr15:78162000-78163000	Weak transcription	Placenta	Placenta
36	chr15:78162200-78163400	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr15:78162400-78162800	Weak transcription	A549	lung
38	chr15:78162400-78163600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr15:78162400-78164800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr15:78162600-78163000	Enhancers	Fetal Kidney	kidney
41	chr15:78162600-78163000	Bivalent Enhancer	Fetal Muscle Leg	muscle
42	chr15:78162600-78163200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr15:78162600-78164400	Bivalent Enhancer	Fetal Stomach	stomach
44	chr15:78162800-78163000	Enhancers	Brain Anterior Caudate	brain
45	chr15:78162800-78163200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
46	chr15:78162800-78163200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr15:78162800-78163200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
48	chr15:78162800-78163200	Enhancers	Pancreas	Pancrea
49	chr15:78162800-78163200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
50	chr15:78162800-78163400	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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