Variant report

Variant	nsv904279
Chromosome Location	chr15:59791666-59842927
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1053)
CpG islands
(count:122)
Chromatin interactive
region (count:25)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1053 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:59825031-59825309	K562	blood:	n/a	n/a
2	ARID3A	chr15:59793838-59793979	K562	blood:	n/a	n/a
3	ATF1	chr15:59827473-59827764	K562	blood:	n/a	n/a
4	ATF1	chr15:59839835-59839910	K562	blood:	n/a	n/a
5	ATF2	chr15:59836001-59836503	GM12878	blood:	n/a	n/a
6	ATF3	chr15:59832054-59832305	K562	blood:	n/a	n/a
7	BACH1	chr15:59836121-59836172	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr15:59821131-59821513	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr15:59836014-59836346	K562	blood:	n/a	n/a
10	BACH1	chr15:59813474-59813485	K562	blood:	n/a	n/a
11	BATF	chr15:59807423-59807696	GM12878	blood:	n/a	chr15:59807516-59807524 chr15:59807611-59807620
12	BATF	chr15:59807420-59807786	GM12878	blood:	n/a	chr15:59807516-59807524 chr15:59807611-59807620
13	BHLHE40	chr15:59825107-59825268	HepG2	liver:	n/a	n/a
14	BHLHE40	chr15:59813612-59813906	GM12878	blood:	n/a	n/a
15	BHLHE40	chr15:59835948-59836366	K562	blood:	n/a	n/a
16	BHLHE40	chr15:59835941-59836377	GM12878	blood:	n/a	n/a
17	BHLHE40	chr15:59825077-59825328	A549	lung:	n/a	n/a
18	BHLHE40	chr15:59808786-59809659	GM12878	blood:	n/a	chr15:59809054-59809075
19	BHLHE40	chr15:59834102-59834272	K562	blood:	n/a	n/a
20	BHLHE40	chr15:59825041-59825112	K562	blood:	n/a	n/a
21	BHLHE40	chr15:59793885-59793953	K562	blood:	n/a	n/a
22	BHLHE40	chr15:59815102-59815397	GM12878	blood:	n/a	n/a
23	BHLHE40	chr15:59842864-59842994	K562	blood:	n/a	n/a
24	BHLHE40	chr15:59809030-59809141	K562	blood:	n/a	chr15:59809054-59809075
25	BRCA1	chr15:59821147-59821435	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr15:59821067-59821470	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr15:59832148-59832177	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr15:59793722-59794037	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr15:59831956-59832291	K562	blood:	n/a	n/a
30	CBX3	chr15:59831999-59832432	HCT-116	colon:	n/a	n/a
31	CBX3	chr15:59836089-59836438	K562	blood:	n/a	n/a
32	CEBPB	chr15:59842868-59843473	Hela-S3	cervix:	n/a	chr15:59843277-59843288 chr15:59843276-59843289
33	CEBPB	chr15:59793747-59794035	K562	blood:	n/a	n/a
34	CEBPB	chr15:59815213-59815685	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr15:59815351-59815572	A549	lung:	n/a	n/a
36	CEBPB	chr15:59835994-59836079	K562	blood:	n/a	n/a
37	CEBPB	chr15:59793713-59794020	HepG2	liver:	n/a	n/a
38	CEBPB	chr15:59821151-59821422	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr15:59793798-59794110	IMR90	lung:	n/a	n/a
40	CEBPB	chr15:59793724-59794079	A549	lung:	n/a	n/a
41	CEBPB	chr15:59793733-59794048	MCF-7	breast:	n/a	n/a
42	CEBPB	chr15:59821239-59821502	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr15:59815152-59815533	K562	blood:	n/a	n/a
44	CEBPB	chr15:59838218-59838437	HepG2	liver:	n/a	n/a
45	CEBPB	chr15:59838223-59838407	HepG2	liver:	n/a	n/a
46	CEBPB	chr15:59815999-59816176	K562	blood:	n/a	n/a
47	CEBPB	chr15:59815182-59815824	ECC-1	luminal epithelium:	n/a	n/a
48	CEBPB	chr15:59815313-59815653	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr15:59793726-59794077	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr15:59832051-59832274	Hela-S3	cervix:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:59841613-59841663	ovcar-3	ovarian:	n/a
2	chr15:59841613-59841663	BJ	skin:	n/a
3	chr15:59841613-59841663	SAEC	small airway:	n/a
4	chr15:59841613-59841663	HRE	kidney:	n/a
5	chr15:59841613-59841663	GM12892	blood:	n/a
6	chr15:59841613-59841663	MCF10A-Er-Src	breast:	n/a
7	chr15:59841613-59841663	HNPCEpiC	eye:	n/a
8	chr15:59841613-59841663	NHBE	bronchial:	n/a
9	chr15:59841613-59841663	AG04450	lung:	fetal
10	chr15:59815173-59815223	HEK293	kidney:	embryo
11	chr15:59815173-59815223	ProgFib	skin:	n/a
12	chr15:59841613-59841663	AoSMC	blood vessel:	n/a
13	chr15:59815173-59815223	HNPCEpiC	eye:	n/a
14	chr15:59815173-59815223	HCF	heart:	n/a
15	chr15:59815173-59815223	HRCEpiC	kidney:	n/a
16	chr15:59841613-59841663	HUVEC	blood vessel:	n/a
17	chr15:59841613-59841663	SKMC	muscle:	n/a
18	chr15:59841613-59841663	NH-A	brain:	n/a
19	chr15:59815173-59815223	GM12892	blood:	n/a
20	chr15:59841613-59841663	HCM	heart:	n/a
21	chr15:59815173-59815223	NHBE	bronchial:	n/a
22	chr15:59815173-59815223	ovcar-3	ovarian:	n/a
23	chr15:59815173-59815223	HIPEpiC	eye:	n/a
24	chr15:59841613-59841663	IMR90	lung:	fetal
25	chr15:59815173-59815223	SKMC	muscle:	n/a
26	chr15:59841613-59841663	MCF-7	breast:	n/a
27	chr15:59841613-59841663	HEK293	kidney:	embryo
28	chr15:59815173-59815223	HUVEC	blood vessel:	n/a
29	chr15:59841613-59841663	HMEC	breast:	n/a
30	chr15:59815173-59815223	PFSK-1	brain:	n/a
31	chr15:59841613-59841663	HepG2	liver:	n/a
32	chr15:59815173-59815223	GM19239	blood:	n/a
33	chr15:59841613-59841663	HPAEpiC	pulmonary alveolar:	n/a
34	chr15:59815173-59815223	AG09309	skin:	n/a
35	chr15:59841613-59841663	Hepatocyte	liver:	n/a
36	chr15:59841613-59841663	HRPEpiC	eye:	n/a
37	chr15:59841613-59841663	SK-N-SH	brain:	n/a
38	chr15:59841613-59841663	A549	lung:	n/a
39	chr15:59815173-59815223	NHDF-neo	bronchial:	n/a
40	chr15:59841613-59841663	NT2-D1	testis:	n/a
41	chr15:59815173-59815223	HRE	kidney:	n/a
42	chr15:59841613-59841663	U87	brain:	n/a
43	chr15:59841613-59841663	H1-hESC	embryonic stem cell:	embryo
44	chr15:59841613-59841663	Caco-2	colon:	n/a
45	chr15:59815173-59815223	HCM	heart:	n/a
46	chr15:59815173-59815223	HEEpiC	esophagus:	n/a
47	chr15:59841613-59841663	GM19239	blood:	n/a
48	chr15:59841613-59841663	HAEpiC	amniotic membrane:	n/a
49	chr15:59815173-59815223	CMK	blood:	n/a
50	chr15:59815173-59815223	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:59800710..59803092-chr15:59806017..59808142,2	K562	blood:
2	chr15:59798477..59800419-chr15:59803208..59805608,2	K562	blood:
3	chr15:59824873..59825654-chr15:59854728..59855447,3	K562	blood:
4	chr15:59824890..59825662-chr15:59908821..59909697,3	MCF-7	breast:
5	chr15:59815837..59817433-chr15:59923383..59925258,2	K562	blood:
6	chr15:59785251..59785790-chr15:59793517..59794379,2	K562	blood:
7	chr15:59397711..59399298-chr15:59819776..59821486,2	K562	blood:
8	chr15:59797880..59799138-chr15:59820448..59821362,3	MCF-7	breast:
9	chr15:59800710..59803092-chr15:59806017..59808142,2	K562	blood:
10	chr15:59430544..59431097-chr15:59793219..59793994,2	K562	blood:
11	chr15:59824741..59825604-chr15:59854999..59855608,3	MCF-7	breast:
12	chr15:58505288..58505802-chr15:59820824..59821742,2	K562	blood:
13	chr15:59453203..59454132-chr15:59793468..59794690,4	K562	blood:
14	chr15:59453184..59454047-chr15:59793375..59794182,4	MCF-7	breast:
15	chr15:59824741..59825345-chr15:59914211..59915184,4	MCF-7	breast:
16	chr15:59798477..59800419-chr15:59803208..59805608,2	K562	blood:
17	chr15:59833463..59836271-chr15:59979637..59981674,2	K562	blood:
18	chr15:59834211..59836892-chr15:59948449..59950575,2	K562	blood:
19	chr15:59824679..59825732-chr15:59924625..59925428,4	MCF-7	breast:
20	chr15:59821926..59823729-chr15:59948340..59950286,2	MCF-7	breast:
21	chr15:59842796..59844336-chr15:59845616..59847879,2	MCF-7	breast:
22	chr15:59797880..59799138-chr15:59820448..59821362,3	MCF-7	breast:
23	chr15:59224290..59226490-chr15:59792486..59794000,2	K562	blood:
24	chr15:59824825..59825602-chr15:59914565..59915171,3	K562	blood:
25	chr15:59836389..59839414-chr15:59841539..59845757,5	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM81A-1	chr15:59835922-59836323	NONHSAT044174
2	lnc-GTF2A2-5	chr15:59817621-59818080	NONHSAT044173

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	FAM81A	hsa-miR-148b-3p	chr15:59814488-59814511
2	FAM81A	hsa-miR-148b-3p	chr15:59814504-59814510
3	FAM81A	hsa-miR-132-3p	chr15:59813890-59813911

Variant related genes	Relation type
ENSG00000243780	TF binding region
ENSG00000243780	CpG island
ENSG00000140299	chromatin interactions
ENSG00000140307	chromatin interactions
ENSG00000137776	chromatin interactions
ENSG00000240238	chromatin interactions
ENSG00000259238	chromatin interactions

Extended variants
information (count: 2306 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2306 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4474632	chr15:59791666-59791667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs527771589	chr15:59791678-59791679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs4390536	chr15:59791730-59791731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564702337	chr15:59791778-59791779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532088160	chr15:59791781-59791782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550502574	chr15:59791816-59791817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs35403756	chr15:59791817-59791818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568721760	chr15:59791916-59791917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112766372	chr15:59791924-59791925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533959445	chr15:59791964-59791965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548132011	chr15:59791980-59791981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs566477782	chr15:59791995-59791996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534101746	chr15:59792010-59792011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538064761	chr15:59792028-59792029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150277795	chr15:59792033-59792034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372646249	chr15:59792035-59792036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550142454	chr15:59792052-59792053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78271397	chr15:59792074-59792075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570616257	chr15:59792090-59792091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553746917	chr15:59792103-59792104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556807628	chr15:59792114-59792115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567905287	chr15:59792120-59792121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556060677	chr15:59792127-59792128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs56336092	chr15:59792157-59792158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535492278	chr15:59792164-59792165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs148984663	chr15:59792196-59792197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs144634250	chr15:59792197-59792198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546271426	chr15:59792225-59792226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs117106040	chr15:59792242-59792243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138599677	chr15:59792298-59792299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191122071	chr15:59792372-59792373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562381943	chr15:59792373-59792374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571466951	chr15:59792418-59792419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576550293	chr15:59792422-59792423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs139017731	chr15:59792468-59792469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs117997253	chr15:59792519-59792520	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs557916517	chr15:59792562-59792563	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs547904308	chr15:59792578-59792579	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs560089718	chr15:59792579-59792580	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs182438508	chr15:59792605-59792606	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs141685109	chr15:59792609-59792610	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs570184194	chr15:59792619-59792620	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs146182663	chr15:59792632-59792633	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs147988850	chr15:59792664-59792665	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs568042990	chr15:59792684-59792685	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs540274512	chr15:59792731-59792732	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs535356389	chr15:59792743-59792744	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs539894368	chr15:59792745-59792746	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs187873320	chr15:59792799-59792800	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs369706901	chr15:59792822-59792823	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	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
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Mental retardation	17124404	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:423 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59785400-59793800	Weak transcription	Fetal Kidney	kidney
2	chr15:59793400-59794000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr15:59794000-59794200	Enhancers	Fetal Kidney	kidney
4	chr15:59798600-59800600	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr15:59798800-59799400	Enhancers	Brain Substantia Nigra	brain
6	chr15:59798800-59802200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr15:59800200-59807600	Weak transcription	Pancreas	Pancrea
8	chr15:59804800-59805000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr15:59804800-59805000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr15:59807000-59808600	Enhancers	GM12878-XiMat	blood
11	chr15:59807000-59818000	Enhancers	Primary B cells from peripheral blood	blood
12	chr15:59807200-59816600	Enhancers	Primary B cells from cord blood	blood
13	chr15:59807600-59807800	Enhancers	Pancreas	Pancrea
14	chr15:59807600-59812200	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr15:59808000-59817600	Weak transcription	Fetal Brain Female	brain
16	chr15:59808200-59808800	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr15:59808400-59808600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr15:59808600-59809400	Enhancers	Primary hematopoietic stem cells	blood
19	chr15:59808600-59810000	Flanking Active TSS	GM12878-XiMat	blood
20	chr15:59808800-59809200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr15:59808800-59809600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr15:59809000-59809400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr15:59809000-59809400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
24	chr15:59809000-59809600	Active TSS	Pancreatic Islets	Pancreatic Islet
25	chr15:59809000-59810200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr15:59809200-59814600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr15:59809400-59813400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr15:59809400-59813600	Weak transcription	Primary hematopoietic stem cells	blood
29	chr15:59809600-59810400	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr15:59810000-59811600	Enhancers	GM12878-XiMat	blood
31	chr15:59810200-59810600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr15:59810200-59810800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr15:59810200-59810800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr15:59810400-59811600	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr15:59810800-59815200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr15:59811600-59812400	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr15:59811600-59813400	Weak transcription	GM12878-XiMat	blood
38	chr15:59812200-59812600	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr15:59812400-59812800	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr15:59812600-59818000	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr15:59812800-59813400	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr15:59813400-59813800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
43	chr15:59813400-59813800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
44	chr15:59813400-59814400	Enhancers	GM12878-XiMat	blood
45	chr15:59813400-59814400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr15:59813600-59813800	Enhancers	Primary hematopoietic stem cells	blood
47	chr15:59813600-59813800	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr15:59813800-59814000	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
49	chr15:59813800-59814800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr15:59813800-59814800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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