Variant report

Variant	nsv550260
Chromosome Location	chr10:27616543-27705855
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:985)
CpG islands
(count:1163)
Chromatin interactive
region (count:17)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:985 , 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	chr10:27629946-27630482	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:27672857-27673169	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:27649547-27649808	K562	blood:	n/a	n/a
4	ATF1	chr10:27649531-27649804	K562	blood:	n/a	n/a
5	BATF	chr10:27633841-27634192	GM12878	blood:	n/a	n/a
6	BATF	chr10:27649564-27649764	GM12878	blood:	n/a	n/a
7	BATF	chr10:27643692-27643988	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	chr10:27649567-27649799	K562	blood:	n/a	n/a
14	BHLHE40	chr10:27649517-27649830	GM12878	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	chr10:27633890-27634818	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	chr10:27649596-27649806	K562	blood:	n/a	n/a
21	CCNT2	chr10:27639061-27639239	K562	blood:	n/a	n/a
22	CEBPB	chr10:27634311-27634682	A549	lung:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
23	CEBPB	chr10:27677693-27677915	MCF-7	breast:	n/a	chr10:27677849-27677860
24	CEBPB	chr10:27649533-27649818	A549	lung:	n/a	chr10:27649675-27649686
25	CEBPB	chr10:27649575-27649846	HepG2	liver:	n/a	chr10:27649675-27649686
26	CEBPB	chr10:27649503-27649883	K562	blood:	n/a	chr10:27649675-27649686
27	CEBPB	chr10:27677675-27678050	Hela-S3	cervix:	n/a	chr10:27677849-27677860
28	CEBPB	chr10:27662837-27663055	K562	blood:	n/a	chr10:27662910-27662921
29	CEBPB	chr10:27672728-27673265	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr10:27677739-27678016	HepG2	liver:	n/a	chr10:27677849-27677860
31	CEBPB	chr10:27655050-27655300	K562	blood:	n/a	chr10:27655162-27655173 chr10:27655161-27655172 chr10:27655161-27655174
32	CEBPB	chr10:27624329-27624377	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr10:27672658-27673316	A549	lung:	n/a	n/a
34	CEBPB	chr10:27684721-27685002	Hela-S3	cervix:	n/a	chr10:27684883-27684896
35	CEBPB	chr10:27672754-27673203	A549	lung:	n/a	n/a
36	CEBPB	chr10:27659541-27659772	HepG2	liver:	n/a	chr10:27659628-27659639 chr10:27659627-27659638 chr10:27659627-27659640
37	CEBPB	chr10:27672755-27673183	A549	lung:	n/a	n/a
38	CEBPB	chr10:27662820-27663067	HepG2	liver:	n/a	chr10:27662910-27662921
39	CEBPB	chr10:27653947-27654086	K562	blood:	n/a	n/a
40	CEBPB	chr10:27680208-27680388	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr10:27649513-27649869	IMR90	lung:	n/a	chr10:27649675-27649686
42	CEBPB	chr10:27634266-27634780	HepG2	liver:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
43	CEBPB	chr10:27677736-27678037	IMR90	lung:	n/a	chr10:27677849-27677860
44	CEBPB	chr10:27634350-27634708	IMR90	lung:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
45	CEBPB	chr10:27634283-27634772	Hela-S3	cervix:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
46	CEBPB	chr10:27679600-27679898	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr10:27669848-27670363	HepG2	liver:	n/a	chr10:27669887-27669899
48	CEBPB	chr10:27655035-27655235	HepG2	liver:	n/a	chr10:27655162-27655173 chr10:27655161-27655172 chr10:27655161-27655174
49	CEBPB	chr10:27672803-27673162	MCF-7	breast:	n/a	n/a
50	CEBPB	chr10:27672818-27673157	HepG2	liver:	n/a	n/a

(count:1163 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:27633745-27633795	NB4	blood:	n/a
2	chr10:27702528-27702578	RPTEC	kidney:	n/a
3	chr10:27703289-27703339	NH-A	brain:	n/a
4	chr10:27704592-27704642	HMEC	breast:	n/a
5	chr10:27633745-27633795	NB4	blood:	n/a
6	chr10:27702528-27702578	RPTEC	kidney:	n/a
7	chr10:27703289-27703339	NH-A	brain:	n/a
8	chr10:27704592-27704642	HMEC	breast:	n/a
9	chr10:27639136-27639186	HEK293	kidney:	embryo
10	chr10:27703486-27703536	MCF10A-Er-Src	breast:	n/a
11	chr10:27703247-27703297	LNCaP	prostate:	n/a
12	chr10:27704762-27704812	RPTEC	kidney:	n/a
13	chr10:27702309-27702359	HIPEpiC	eye:	n/a
14	chr10:27703336-27703386	GM06990	blood:	n/a
15	chr10:27703362-27703412	HL-60	blood:	n/a
16	chr10:27633745-27633795	AG04449	skin:	fetal
17	chr10:27703329-27703379	HCM	heart:	n/a
18	chr10:27704762-27704812	NHDF-neo	bronchial:	n/a
19	chr10:27703547-27703597	MCF10A-Er-Src	breast:	n/a
20	chr10:27633745-27633795	HCPEpiC	choroid plexus:	n/a
21	chr10:27639136-27639186	NT2-D1	testis:	n/a
22	chr10:27698606-27698656	GM12891	blood:	n/a
23	chr10:27702309-27702359	HEK293	kidney:	embryo
24	chr10:27702309-27702359	SK-N-SH_RA	brain:	n/a
25	chr10:27703247-27703297	PrEC	prostate:	n/a
26	chr10:27702774-27702824	NHDF-neo	bronchial:	n/a
27	chr10:27703336-27703386	NHBE	bronchial:	n/a
28	chr10:27634719-27634769	SK-N-SH_RA	brain:	n/a
29	chr10:27704762-27704812	Jurkat	blood:	n/a
30	chr10:27703329-27703379	CMK	blood:	n/a
31	chr10:27703247-27703297	GM06990	blood:	n/a
32	chr10:27703247-27703297	SAEC	small airway:	n/a
33	chr10:27702309-27702359	PrEC	prostate:	n/a
34	chr10:27704762-27704812	GM12891	blood:	n/a
35	chr10:27702528-27702578	NHBE	bronchial:	n/a
36	chr10:27704592-27704642	AG04449	skin:	fetal
37	chr10:27703486-27703536	HRE	kidney:	n/a
38	chr10:27634719-27634769	SK-N-MC	brain:	n/a
39	chr10:27703362-27703412	NT2-D1	testis:	n/a
40	chr10:27703289-27703339	ProgFib	skin:	n/a
41	chr10:27703336-27703386	K562	blood:	n/a
42	chr10:27704762-27704812	HCM	heart:	n/a
43	chr10:27703329-27703379	NB4	blood:	n/a
44	chr10:27703362-27703412	HRCEpiC	kidney:	n/a
45	chr10:27639156-27639206	NB4	blood:	n/a
46	chr10:27704592-27704642	GM06990	blood:	n/a
47	chr10:27703289-27703339	SK-N-MC	brain:	n/a
48	chr10:27703377-27703427	AG10803	skin:	n/a
49	chr10:27639136-27639186	SKMC	muscle:	n/a
50	chr10:27702528-27702578	GM19239	blood:	n/a

(count:17 , 50 per page) page: 1

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

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

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

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
TRIAP1P1	TF binding region
RNU6-452P	TF binding region
PTCHD3	TF binding region
FAM210CP	TF binding region
ENSG00000260151	TF binding region
ENSG00000215409	TF binding region
TRIAP1P1	CpG island
RNU6-452P	CpG island
PTCHD3	CpG island
FAM210CP	CpG island
ENSG00000260151	CpG island
ENSG00000215409	CpG island
ENSG00000107897	chromatin interactions
ENSG00000262412	chromatin interactions
ENSG00000136758	chromatin interactions
ENSG00000099246	chromatin interactions
ENSG00000182077	chromatin interactions
ENSG00000120539	chromatin interactions

Extended variants
information (count: 2565 )
Associated
traits (count: 46 )

Variant overlapped rSNPs/rCNVs (count:2565 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11015696	chr10:27616543-27616544	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569353422	chr10:27616551-27616552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535103538	chr10:27616558-27616559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144038479	chr10:27616584-27616585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575018528	chr10:27616590-27616591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540888564	chr10:27616599-27616600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554426307	chr10:27616624-27616625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577464824	chr10:27616653-27616654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546325619	chr10:27616727-27616728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs193246477	chr10:27616747-27616748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs148653231	chr10:27616805-27616806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541834398	chr10:27616869-27616870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112284973	chr10:27616879-27616880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs367604818	chr10:27616883-27616884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112747474	chr10:27616889-27616890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139899401	chr10:27616949-27616950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145341675	chr10:27616981-27616982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576611858	chr10:27617014-27617015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569392753	chr10:27617028-27617029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185214873	chr10:27617034-27617035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs187374821	chr10:27617062-27617063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12250366	chr10:27617073-27617074	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs538930955	chr10:27617121-27617122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs151027221	chr10:27617130-27617131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141099980	chr10:27617201-27617202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570140102	chr10:27617233-27617234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs237590	chr10:27617246-27617247	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs11015697	chr10:27617379-27617380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540969103	chr10:27617815-27617816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184017496	chr10:27617836-27617837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs532989947	chr10:27617847-27617848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538089438	chr10:27617852-27617853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs549550941	chr10:27617854-27617855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551279839	chr10:27617883-27617884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563466028	chr10:27617966-27617967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs529003173	chr10:27617996-27617997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544929759	chr10:27618050-27618051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373198065	chr10:27618087-27618088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188604587	chr10:27618107-27618108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549014110	chr10:27618124-27618125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs111339129	chr10:27618224-27618225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534599179	chr10:27618250-27618251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs12261747	chr10:27618287-27618288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs548153391	chr10:27618339-27618340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs79310920	chr10:27618403-27618404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540071739	chr10:27618419-27618420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184455815	chr10:27618452-27618453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576550657	chr10:27618463-27618464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs78713529	chr10:27618539-27618540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535586856	chr10:27618542-27618543	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:295 , 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	chr10:27617800-27618400	Enhancers	Fetal Intestine Large	intestine
3	chr10:27618400-27619600	Weak transcription	Fetal Intestine Large	intestine
4	chr10:27619400-27619600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr10:27619400-27620200	Enhancers	Fetal Intestine Small	intestine
6	chr10:27619600-27619800	Enhancers	Fetal Intestine Large	intestine
7	chr10:27623400-27624800	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr10:27624200-27624800	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr10:27625800-27626200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr10:27626600-27627400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr10:27629600-27630400	Enhancers	HepG2	liver
12	chr10:27629800-27630200	Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr10:27630200-27630400	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr10:27630400-27631000	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr10:27633400-27634000	Enhancers	Brain Germinal Matrix	brain
16	chr10:27633400-27634400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr10:27633400-27634400	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr10:27633400-27634600	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr10:27633400-27634800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr10:27633600-27633800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr10:27633600-27634000	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr10:27633600-27634000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr10:27633600-27634000	Enhancers	GM12878-XiMat	blood
24	chr10:27633600-27634600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr10:27633600-27634800	Enhancers	Fetal Muscle Leg	muscle
26	chr10:27633800-27634400	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr10:27633800-27655400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr10:27634000-27634400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr10:27634000-27634400	Flanking Active TSS	Brain Germinal Matrix	brain
30	chr10:27634000-27634600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr10:27634000-27634600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
32	chr10:27634000-27634600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr10:27634000-27634800	Flanking Active TSS	GM12878-XiMat	blood
34	chr10:27634200-27634600	Enhancers	Primary B cells from peripheral blood	blood
35	chr10:27634200-27634600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr10:27634200-27634600	Enhancers	Right Atrium	heart
37	chr10:27634200-27634800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr10:27634200-27635400	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr10:27634200-27635400	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr10:27634400-27634600	Enhancers	Adipose Nuclei	Adipose
41	chr10:27634400-27634800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
42	chr10:27634400-27634800	Enhancers	Brain Germinal Matrix	brain
43	chr10:27634400-27635400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr10:27634400-27636400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr10:27634400-27636600	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr10:27634600-27634800	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr10:27634600-27634800	Enhancers	Dnd41	blood
48	chr10:27634600-27635200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr10:27634600-27639600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr10:27634600-27643200	Weak transcription	Right Atrium	heart

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