Variant report

Variant	nsv430151
Chromosome Location	chr10:27615394-27701894
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:962)
CpG islands
(count:305)
Chromatin interactive
region (count:18)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:962 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:27649547-27649808	K562	blood:	n/a	n/a
2	ARID3A	chr10:27629946-27630482	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:27672857-27673169	HepG2	liver:	n/a	n/a
4	ATF1	chr10:27649531-27649804	K562	blood:	n/a	n/a
5	BATF	chr10:27643692-27643988	GM12878	blood:	n/a	n/a
6	BATF	chr10:27633841-27634192	GM12878	blood:	n/a	n/a
7	BATF	chr10:27649564-27649764	GM12878	blood:	n/a	n/a
8	BCL11A	chr10:27643724-27643987	GM12878	blood:	n/a	n/a
9	BCL11A	chr10:27643658-27644039	GM12878	blood:	n/a	n/a
10	BCL3	chr10:27672617-27673252	A549	lung:	n/a	n/a
11	BCLAF1	chr10:27643572-27643923	GM12878	blood:	n/a	n/a
12	BHLHE40	chr10:27672558-27673044	HepG2	liver:	n/a	n/a
13	BHLHE40	chr10:27633890-27634818	GM12878	blood:	n/a	n/a
14	BHLHE40	chr10:27649567-27649799	K562	blood:	n/a	n/a
15	BHLHE40	chr10:27646116-27646388	K562	blood:	n/a	chr10:27646219-27646232 chr10:27646221-27646230 chr10:27646222-27646231 chr10:27646221-27646230
16	BHLHE40	chr10:27649517-27649830	GM12878	blood:	n/a	n/a
17	BRCA1	chr10:27672817-27673127	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr10:27681602-27681815	K562	blood:	n/a	n/a
19	CBX3	chr10:27681617-27681837	K562	blood:	n/a	n/a
20	CCNT2	chr10:27639061-27639239	K562	blood:	n/a	n/a
21	CCNT2	chr10:27649596-27649806	K562	blood:	n/a	n/a
22	CEBPB	chr10:27677739-27678016	HepG2	liver:	n/a	chr10:27677849-27677860
23	CEBPB	chr10:27672658-27673316	A549	lung:	n/a	n/a
24	CEBPB	chr10:27649575-27649846	HepG2	liver:	n/a	chr10:27649675-27649686
25	CEBPB	chr10:27662820-27663067	HepG2	liver:	n/a	chr10:27662910-27662921
26	CEBPB	chr10:27659541-27659772	HepG2	liver:	n/a	chr10:27659628-27659639 chr10:27659627-27659638 chr10:27659627-27659640
27	CEBPB	chr10:27634350-27634708	IMR90	lung:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
28	CEBPB	chr10:27624329-27624377	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr10:27677675-27678050	Hela-S3	cervix:	n/a	chr10:27677849-27677860
30	CEBPB	chr10:27672754-27673203	A549	lung:	n/a	n/a
31	CEBPB	chr10:27634283-27634772	Hela-S3	cervix:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
32	CEBPB	chr10:27649533-27649818	A549	lung:	n/a	chr10:27649675-27649686
33	CEBPB	chr10:27672755-27673183	A549	lung:	n/a	n/a
34	CEBPB	chr10:27669848-27670363	HepG2	liver:	n/a	chr10:27669887-27669899
35	CEBPB	chr10:27677736-27678037	IMR90	lung:	n/a	chr10:27677849-27677860
36	CEBPB	chr10:27679600-27679898	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr10:27634311-27634682	A549	lung:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
38	CEBPB	chr10:27655050-27655300	K562	blood:	n/a	chr10:27655162-27655173 chr10:27655161-27655172 chr10:27655161-27655174
39	CEBPB	chr10:27672818-27673157	HepG2	liver:	n/a	n/a
40	CEBPB	chr10:27655035-27655235	HepG2	liver:	n/a	chr10:27655162-27655173 chr10:27655161-27655172 chr10:27655161-27655174
41	CEBPB	chr10:27649503-27649883	K562	blood:	n/a	chr10:27649675-27649686
42	CEBPB	chr10:27672728-27673265	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr10:27672803-27673162	MCF-7	breast:	n/a	n/a
44	CEBPB	chr10:27653947-27654086	K562	blood:	n/a	n/a
45	CEBPB	chr10:27684721-27685002	Hela-S3	cervix:	n/a	chr10:27684883-27684896
46	CEBPB	chr10:27662837-27663055	K562	blood:	n/a	chr10:27662910-27662921
47	CEBPB	chr10:27634266-27634780	HepG2	liver:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
48	CEBPB	chr10:27649513-27649869	IMR90	lung:	n/a	chr10:27649675-27649686
49	CEBPB	chr10:27680208-27680388	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr10:27677693-27677915	MCF-7	breast:	n/a	chr10:27677849-27677860

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:27639156-27639206	AoSMC	blood vessel:	n/a
2	chr10:27698606-27698656	MCF-7	breast:	n/a
3	chr10:27633745-27633795	PrEC	prostate:	n/a
4	chr10:27639156-27639206	AG10803	skin:	n/a
5	chr10:27639136-27639186	Jurkat	blood:	n/a
6	chr10:27698606-27698656	H1-hESC	embryonic stem cell:	embryo
7	chr10:27639136-27639186	SK-N-SH	brain:	n/a
8	chr10:27634719-27634769	SK-N-MC	brain:	n/a
9	chr10:27639156-27639206	AG09319	gingival:	n/a
10	chr10:27634719-27634769	Hepatocyte	liver:	n/a
11	chr10:27634719-27634769	AG04449	skin:	fetal
12	chr10:27633745-27633795	ProgFib	skin:	n/a
13	chr10:27698606-27698656	HPAEpiC	pulmonary alveolar:	n/a
14	chr10:27698606-27698656	MCF10A-Er-Src	breast:	n/a
15	chr10:27634719-27634769	CMK	blood:	n/a
16	chr10:27634719-27634769	AG04450	lung:	fetal
17	chr10:27633745-27633795	HCM	heart:	n/a
18	chr10:27698606-27698656	NT2-D1	testis:	n/a
19	chr10:27633745-27633795	U87	brain:	n/a
20	chr10:27633745-27633795	AG09309	skin:	n/a
21	chr10:27633745-27633795	IMR90	lung:	fetal
22	chr10:27639136-27639186	MCF-7	breast:	n/a
23	chr10:27639156-27639206	HNPCEpiC	eye:	n/a
24	chr10:27639136-27639186	H1-hESC	embryonic stem cell:	embryo
25	chr10:27633745-27633795	H1-hESC	embryonic stem cell:	embryo
26	chr10:27634719-27634769	NHDF-neo	bronchial:	n/a
27	chr10:27633745-27633795	HCT-116	colon:	n/a
28	chr10:27634719-27634769	GM12878	blood:	n/a
29	chr10:27634719-27634769	HNPCEpiC	eye:	n/a
30	chr10:27639156-27639206	SAEC	small airway:	n/a
31	chr10:27639156-27639206	GM12878	blood:	n/a
32	chr10:27633745-27633795	HIPEpiC	eye:	n/a
33	chr10:27639156-27639206	HEK293	kidney:	embryo
34	chr10:27698606-27698656	AG09309	skin:	n/a
35	chr10:27633745-27633795	RPTEC	kidney:	n/a
36	chr10:27634719-27634769	MCF-7	breast:	n/a
37	chr10:27639136-27639186	HCPEpiC	choroid plexus:	n/a
38	chr10:27633745-27633795	NHBE	bronchial:	n/a
39	chr10:27633745-27633795	HRPEpiC	eye:	n/a
40	chr10:27639136-27639186	GM19239	blood:	n/a
41	chr10:27634719-27634769	AG10803	skin:	n/a
42	chr10:27634719-27634769	T-47D	breast:	n/a
43	chr10:27634719-27634769	Jurkat	blood:	n/a
44	chr10:27639156-27639206	MCF10A-Er-Src	breast:	n/a
45	chr10:27633745-27633795	HEK293	kidney:	embryo
46	chr10:27633745-27633795	GM06990	blood:	n/a
47	chr10:27698606-27698656	GM19239	blood:	n/a
48	chr10:27639156-27639206	ovcar-3	ovarian:	n/a
49	chr10:27634719-27634769	PANC-1	pancreas:	n/a
50	chr10:27634719-27634769	HUVEC	blood vessel:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:27694442..27697083-chr10:27703247..27705702,3	K562	blood:
2	chr10:27669052..27671269-chr10:27683257..27685068,2	K562	blood:
3	chr10:27441984..27445191-chr10:27642152..27645235,3	MCF-7	breast:
4	chr10:27684512..27686768-chr10:27700849..27702736,2	K562	blood:
5	chr10:27669052..27671269-chr10:27683257..27685068,2	K562	blood:
6	chr10:27684512..27686768-chr10:27700849..27702736,2	K562	blood:
7	chr10:27640371..27642415-chr10:27644846..27646556,2	K562	blood:
8	chr10:27527860..27530153-chr10:27647076..27648802,2	MCF-7	breast:
9	chr10:27529763..27532096-chr10:27643724..27645777,2	MCF-7	breast:
10	chr10:27659927..27662822-chr10:27662832..27664720,3	K562	blood:
11	chr10:27659175..27661663-chr10:27792060..27794224,2	MCF-7	breast:
12	chr10:27659927..27662822-chr10:27662832..27664720,3	K562	blood:
13	chr10:27530526..27532390-chr10:27644695..27646372,2	MCF-7	breast:
14	chr10:27681780..27685010-chr10:27685683..27688279,3	K562	blood:
15	chr10:27681780..27685010-chr10:27685683..27688279,3	K562	blood:
16	chr10:27640371..27642415-chr10:27644846..27646556,2	K562	blood:
17	chr10:27609103..27610966-chr10:27614340..27616128,2	K562	blood:
18	chr10:27531028..27532588-chr10:27647976..27649755,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTCHD3-1	chr10:27667067-27667291	NONHSAT011904
2	lnc-PTCHD3-2	chr10:27627369-27627692	l_277_chr10:27627368-27636725_testes
3	lnc-MASTL-2	chr10:27632365-27633580	ENSG00000260151.1
4	lnc-PTCHD3-2	chr10:27634694-27635239	l_277_chr10:27627368-27636725_testes
5	lnc-MASTL-2	chr10:27633668-27633846	ENSG00000260151.1
6	lnc-PTCHD3-2	chr10:27636298-27636725	l_277_chr10:27627368-27636725_testes

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PTCHD3	hsa-miR-128-3p	chr10:27687123-27687143

Variant related genes	Relation type
FAM210CP	TF binding region
ENSG00000260151	TF binding region
TRIAP1P1	TF binding region
RNU6-452P	TF binding region
ENSG00000215409	TF binding region
FAM210CP	CpG island
ENSG00000260151	CpG island
TRIAP1P1	CpG island
RNU6-452P	CpG island
ENSG00000215409	CpG island
ENSG00000262412	chromatin interactions
ENSG00000099246	chromatin interactions
ENSG00000136758	chromatin interactions
ENSG00000107897	chromatin interactions
ENSG00000182077	chromatin interactions
ENSG00000120539	chromatin interactions

Extended variants
information (count: 2395 )
Associated
traits (count: 46 )

Variant overlapped rSNPs/rCNVs (count:2395 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186925126	chr10:27615395-27615396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs373154143	chr10:27615427-27615428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs16927215	chr10:27615437-27615438	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs11015695	chr10:27615461-27615462	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs575549785	chr10:27615462-27615463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190140796	chr10:27615493-27615494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144711126	chr10:27615501-27615502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577049144	chr10:27615514-27615515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182374775	chr10:27615527-27615528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544065497	chr10:27615533-27615534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs76734853	chr10:27615538-27615539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530194551	chr10:27615574-27615575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115871030	chr10:27615577-27615578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560383021	chr10:27615586-27615587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs186711458	chr10:27615592-27615593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138553113	chr10:27615613-27615614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536870255	chr10:27615630-27615631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538158265	chr10:27615754-27615755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548134928	chr10:27615755-27615756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568252527	chr10:27615756-27615757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533738777	chr10:27615759-27615760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189850828	chr10:27615763-27615764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141509383	chr10:27615810-27615811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115240951	chr10:27615825-27615826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569132	chr10:27615832-27615833	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs529790157	chr10:27615852-27615853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149302182	chr10:27615868-27615869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs556387811	chr10:27615898-27615899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537401519	chr10:27615910-27615911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575586850	chr10:27615951-27615952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549980953	chr10:27615961-27615962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561415498	chr10:27615977-27615978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182752417	chr10:27615984-27615985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567331	chr10:27616001-27616002	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs560604798	chr10:27616054-27616055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532665920	chr10:27616070-27616071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs202191914	chr10:27616072-27616073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563383324	chr10:27616077-27616078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371664218	chr10:27616078-27616079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531430787	chr10:27616079-27616080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371408401	chr10:27616092-27616093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112652867	chr10:27616093-27616094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114925811	chr10:27616125-27616126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566288	chr10:27616140-27616141	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs565560	chr10:27616171-27616172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188967254	chr10:27616184-27616185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548503481	chr10:27616266-27616267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554220065	chr10:27616329-27616330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs527507443	chr10:27616370-27616371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs149528493	chr10:27616443-27616444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:46)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Autism	21439084	CNVD
Maculopathy	20981449	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21525872	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27613400-27617400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr10:27616200-27616400	Enhancers	Fetal Thymus	thymus
3	chr10:27617800-27618400	Enhancers	Fetal Intestine Large	intestine
4	chr10:27618400-27619600	Weak transcription	Fetal Intestine Large	intestine
5	chr10:27619400-27619600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr10:27619400-27620200	Enhancers	Fetal Intestine Small	intestine
7	chr10:27619600-27619800	Enhancers	Fetal Intestine Large	intestine
8	chr10:27623400-27624800	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr10:27624200-27624800	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr10:27625800-27626200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr10:27626600-27627400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr10:27629600-27630400	Enhancers	HepG2	liver
13	chr10:27629800-27630200	Active TSS	Pancreatic Islets	Pancreatic Islet
14	chr10:27630200-27630400	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr10:27630400-27631000	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr10:27633400-27634000	Enhancers	Brain Germinal Matrix	brain
17	chr10:27633400-27634400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr10:27633400-27634400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr10:27633400-27634600	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr10:27633400-27634800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr10:27633600-27633800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr10:27633600-27634000	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr10:27633600-27634000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr10:27633600-27634000	Enhancers	GM12878-XiMat	blood
25	chr10:27633600-27634600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr10:27633600-27634800	Enhancers	Fetal Muscle Leg	muscle
27	chr10:27633800-27634400	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr10:27633800-27655400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr10:27634000-27634400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr10:27634000-27634400	Flanking Active TSS	Brain Germinal Matrix	brain
31	chr10:27634000-27634600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr10:27634000-27634600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
33	chr10:27634000-27634600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr10:27634000-27634800	Flanking Active TSS	GM12878-XiMat	blood
35	chr10:27634200-27634600	Enhancers	Primary B cells from peripheral blood	blood
36	chr10:27634200-27634600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr10:27634200-27634600	Enhancers	Right Atrium	heart
38	chr10:27634200-27634800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr10:27634200-27635400	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr10:27634200-27635400	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr10:27634400-27634600	Enhancers	Adipose Nuclei	Adipose
42	chr10:27634400-27634800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
43	chr10:27634400-27634800	Enhancers	Brain Germinal Matrix	brain
44	chr10:27634400-27635400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr10:27634400-27636400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr10:27634400-27636600	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr10:27634600-27634800	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr10:27634600-27634800	Enhancers	Dnd41	blood
49	chr10:27634600-27635200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr10:27634600-27639600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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