Variant report

Variant	nsv895370
Chromosome Location	chr10:49421173-49484698
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:641)
CpG islands
(count:733)
Chromatin interactive
region (count:36)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:641 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr10:49433149-49433416	K562	blood:	n/a	n/a
2	ATF2	chr10:49439298-49440117	GM12878	blood:	n/a	n/a
3	BATF	chr10:49439308-49439566	GM12878	blood:	n/a	n/a
4	BATF	chr10:49480732-49481076	GM12878	blood:	n/a	n/a
5	BATF	chr10:49474596-49474854	GM12878	blood:	n/a	n/a
6	BATF	chr10:49480801-49481052	GM12878	blood:	n/a	n/a
7	BATF	chr10:49474491-49474913	GM12878	blood:	n/a	n/a
8	BCL11A	chr10:49439692-49440093	GM12878	blood:	n/a	n/a
9	BHLHE40	chr10:49464070-49464101	K562	blood:	n/a	n/a
10	BHLHE40	chr10:49423560-49423845	GM12878	blood:	n/a	n/a
11	BRCA1	chr10:49440180-49440230	GM12878	blood:	n/a	n/a
12	BRCA1	chr10:49423544-49423673	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr10:49435560-49435564	GM12878	blood:	n/a	n/a
14	CEBPB	chr10:49474673-49474895	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr10:49474655-49474929	K562	blood:	n/a	n/a
16	CEBPB	chr10:49484362-49484594	IMR90	lung:	n/a	chr10:49484442-49484453 chr10:49484442-49484455
17	CEBPB	chr10:49466370-49466438	H1-hESC	embryonic stem cell:	n/a	chr10:49466401-49466414 chr10:49466401-49466412
18	CEBPB	chr10:49475926-49475958	K562	blood:	n/a	n/a
19	CEBPB	chr10:49466240-49466563	HepG2	liver:	n/a	chr10:49466401-49466414 chr10:49466401-49466412
20	CEBPB	chr10:49480965-49481230	K562	blood:	n/a	chr10:49481108-49481119
21	CEBPB	chr10:49484362-49484595	A549	lung:	n/a	chr10:49484442-49484453 chr10:49484442-49484455
22	CEBPB	chr10:49423528-49423831	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr10:49474695-49474936	A549	lung:	n/a	n/a
24	CEBPB	chr10:49448772-49449059	K562	blood:	n/a	chr10:49448913-49448924
25	CEBPB	chr10:49474701-49474888	HepG2	liver:	n/a	n/a
26	CEBPB	chr10:49466317-49466554	K562	blood:	n/a	chr10:49466401-49466414 chr10:49466401-49466412
27	CEBPB	chr10:49484304-49484565	K562	blood:	n/a	chr10:49484442-49484453 chr10:49484442-49484455
28	CEBPB	chr10:49484299-49484611	HepG2	liver:	n/a	chr10:49484442-49484453 chr10:49484442-49484455
29	CEBPB	chr10:49421408-49421558	A549	lung:	n/a	n/a
30	CEBPB	chr10:49448853-49448934	HepG2	liver:	n/a	chr10:49448913-49448924
31	CEBPB	chr10:49459270-49459470	HepG2	liver:	n/a	n/a
32	CEBPB	chr10:49481008-49481212	A549	lung:	n/a	chr10:49481108-49481119
33	CEBPB	chr10:49480990-49481283	HepG2	liver:	n/a	chr10:49481108-49481119
34	CHD2	chr10:49440033-49440075	GM12878	blood:	n/a	n/a
35	CTCF	chr10:49423620-49423770	SAEC	small airway:	n/a	chr10:49423685-49423703 chr10:49423687-49423708 chr10:49423688-49423701
36	CTCF	chr10:49423580-49423850	A549	lung:	n/a	chr10:49423685-49423703 chr10:49423687-49423708 chr10:49423688-49423701
37	CTCF	chr10:49474700-49474850	GM12868	blood:	n/a	n/a
38	CTCF	chr10:49423980-49424130	HAc	cerebellar:	n/a	n/a
39	CTCF	chr10:49423600-49423750	GM06990	blood:	n/a	chr10:49423685-49423703 chr10:49423687-49423708 chr10:49423688-49423701
40	CTCF	chr10:49423353-49423437	Gliobla	brain:	n/a	n/a
41	CTCF	chr10:49423357-49423972	HCT-116	colon:	n/a	chr10:49423685-49423703 chr10:49423687-49423708 chr10:49423688-49423701
42	CTCF	chr10:49423600-49423750	GM12870	blood:	n/a	chr10:49423685-49423703 chr10:49423687-49423708 chr10:49423688-49423701
43	CTCF	chr10:49441760-49441910	GM12864	blood:	n/a	n/a
44	CTCF	chr10:49423640-49423790	AG09309	skin:	n/a	chr10:49423685-49423703 chr10:49423687-49423708 chr10:49423688-49423701
45	CTCF	chr10:49474620-49474770	GM12871	blood:	n/a	n/a
46	CTCF	chr10:49474660-49474810	GM12869	blood:	n/a	n/a
47	CTCF	chr10:49441883-49441944	GM10248	blood:	n/a	n/a
48	CTCF	chr10:49455500-49455650	GM12866	blood:	n/a	n/a
49	CTCF	chr10:49474660-49474810	GM12873	blood:	n/a	n/a
50	CTCF	chr10:49423620-49423770	BJ	skin:	n/a	chr10:49423685-49423703 chr10:49423687-49423708 chr10:49423688-49423701

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:49482695-49482745	HEK293	kidney:	embryo
2	chr10:49482695-49482745	HEK293	kidney:	embryo
3	chr10:49444466-49444516	U87	brain:	n/a
4	chr10:49460154-49460204	HCT-116	colon:	n/a
5	chr10:49482723-49482773	Jurkat	blood:	n/a
6	chr10:49482826-49482876	MCF-7	breast:	n/a
7	chr10:49482871-49482921	ECC-1	luminal epithelium:	n/a
8	chr10:49459949-49459999	GM12892	blood:	n/a
9	chr10:49460154-49460204	SK-N-SH	brain:	n/a
10	chr10:49459949-49459999	HCF	heart:	n/a
11	chr10:49444466-49444516	CMK	blood:	n/a
12	chr10:49444466-49444516	SKMC	muscle:	n/a
13	chr10:49460249-49460299	PrEC	prostate:	n/a
14	chr10:49483356-49483406	Hepatocyte	liver:	n/a
15	chr10:49482871-49482921	SK-N-MC	brain:	n/a
16	chr10:49459949-49459999	HCM	heart:	n/a
17	chr10:49459949-49459999	NHBE	bronchial:	n/a
18	chr10:49459949-49459999	Hepatocyte	liver:	n/a
19	chr10:49483356-49483406	HRCEpiC	kidney:	n/a
20	chr10:49482723-49482773	HMEC	breast:	n/a
21	chr10:49444466-49444516	HepG2	liver:	n/a
22	chr10:49482826-49482876	HCPEpiC	choroid plexus:	n/a
23	chr10:49483700-49483750	SK-N-SH_RA	brain:	n/a
24	chr10:49459800-49459850	HEEpiC	esophagus:	n/a
25	chr10:49483700-49483750	K562	blood:	n/a
26	chr10:49482767-49482817	H1-hESC	embryonic stem cell:	embryo
27	chr10:49482767-49482817	K562	blood:	n/a
28	chr10:49482871-49482921	U87	brain:	n/a
29	chr10:49482871-49482921	Caco-2	colon:	n/a
30	chr10:49460154-49460204	HEK293	kidney:	embryo
31	chr10:49482695-49482745	HPAEpiC	pulmonary alveolar:	n/a
32	chr10:49459800-49459850	GM12878	blood:	n/a
33	chr10:49483356-49483406	HepG2	liver:	n/a
34	chr10:49482767-49482817	NH-A	brain:	n/a
35	chr10:49482767-49482817	GM19239	blood:	n/a
36	chr10:49482826-49482876	HepG2	liver:	n/a
37	chr10:49482695-49482745	AG04449	skin:	fetal
38	chr10:49460154-49460204	AG04449	skin:	fetal
39	chr10:49459949-49459999	AG09309	skin:	n/a
40	chr10:49482767-49482817	ProgFib	skin:	n/a
41	chr10:49482767-49482817	A549	lung:	n/a
42	chr10:49482826-49482876	NB4	blood:	n/a
43	chr10:49460154-49460204	Hela-S3	cervix:	n/a
44	chr10:49483700-49483750	H1-hESC	embryonic stem cell:	embryo
45	chr10:49482826-49482876	CMK	blood:	n/a
46	chr10:49460154-49460204	HAEpiC	amniotic membrane:	n/a
47	chr10:49483700-49483750	HUVEC	blood vessel:	n/a
48	chr10:49482826-49482876	PrEC	prostate:	n/a
49	chr10:49459949-49459999	GM06990	blood:	n/a
50	chr10:49460249-49460299	HPAEpiC	pulmonary alveolar:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:49441878..49444791-chr10:49513078..49515110,2	K562	blood:
2	chr10:49422440..49425186-chr10:49494550..49500073,5	MCF-7	breast:
3	chr10:49455171..49459058-chr10:49459196..49462154,3	K562	blood:
4	chr10:49455171..49457750-chr10:49459859..49462154,2	K562	blood:
5	chr10:49475447..49477971-chr10:49480331..49482798,2	K562	blood:
6	chr10:49430760..49432504-chr10:49497937..49500737,2	K562	blood:
7	chr10:49423588..49424151-chr10:49714065..49715162,3	MCF-7	breast:
8	chr10:49460728..49464367-chr10:49465892..49469453,3	K562	blood:
9	chr10:49423548..49424230-chr10:49863873..49864448,2	K562	blood:
10	chr10:49461805..49464340-chr10:49481362..49483137,2	K562	blood:
11	chr10:49442419..49445275-chr10:49506224..49508061,2	K562	blood:
12	chr10:49423481..49424232-chr10:49497847..49498349,2	K562	blood:
13	chr10:49423127..49424126-chr10:49497102..49498218,5	MCF-7	breast:
14	chr10:49433973..49437325-chr10:49440787..49445569,4	K562	blood:
15	chr10:49475447..49477972-chr10:49481298..49483019,2	K562	blood:
16	chr10:49438438..49440728-chr10:49443853..49445839,2	K562	blood:
17	chr10:49423144..49424160-chr10:49497116..49498379,10	MCF-7	breast:
18	chr10:49455241..49456959-chr10:49462949..49465290,2	MCF-7	breast:
19	chr10:49451828..49454602-chr10:49458352..49460279,2	K562	blood:
20	chr10:49459652..49462139-chr10:49513267..49515617,2	K562	blood:
21	chr10:49464368..49465891-chr10:49470466..49472102,2	MCF-7	breast:
22	chr10:49398931..49401255-chr10:49429672..49432086,2	K562	blood:
23	chr10:49433973..49437325-chr10:49440787..49445569,4	K562	blood:
24	chr10:49414468..49419005-chr10:49423679..49427949,4	K562	blood:
25	chr10:49423270..49424166-chr10:49714289..49715192,4	K562	blood:
26	chr10:49438433..49440728-chr10:49443022..49446570,3	K562	blood:
27	chr10:49423310..49424126-chr10:49540299..49540827,2	MCF-7	breast:
28	chr10:49438433..49440728-chr10:49443022..49446570,3	K562	blood:
29	chr10:49460728..49464367-chr10:49465892..49469453,3	K562	blood:
30	chr10:49455241..49456959-chr10:49462949..49465290,2	MCF-7	breast:
31	chr10:49419791..49421477-chr10:49492128..49494569,2	K562	blood:
32	chr10:49455171..49457750-chr10:49459859..49462154,2	K562	blood:
33	chr10:49414468..49418793-chr10:49423679..49426769,3	K562	blood:
34	chr10:49438438..49440728-chr10:49443853..49445839,2	K562	blood:
35	chr10:49464368..49465891-chr10:49470466..49472102,2	MCF-7	breast:
36	chr10:49462023..49464427-chr10:49493283..49495844,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAPK8-4	chr10:49456119-49456389	NONHSAT013262
2	lnc-MAPK8-4	chr10:49455216-49455941	NONHSAT013262
3	lnc-PTPN20C-7	chr10:49456586-49457221	NONHSAT013263
4	lnc-PTPN20C-7	chr10:49459609-49459654	NONHSAT013263

No data

Variant related genes	Relation type
FRMPD2	TF binding region
FRMPD2	CpG island
ENSG00000170324	chromatin interactions
ENSG00000107643	chromatin interactions
ENSG00000128805	chromatin interactions

Extended variants
information (count: 2598 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2598 , 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	rs10857549	chr10:49421173-49421174	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs375754353	chr10:49421182-49421183	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148072975	chr10:49421201-49421202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540048011	chr10:49421294-49421295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs11101265	chr10:49421299-49421300	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs186783649	chr10:49421308-49421309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545396742	chr10:49421309-49421310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376754063	chr10:49421317-49421318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146010671	chr10:49421325-49421326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574185656	chr10:49421371-49421372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531132355	chr10:49421412-49421413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548342875	chr10:49421461-49421462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs79458128	chr10:49421477-49421478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558111215	chr10:49421494-49421495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs76037323	chr10:49421529-49421530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs367891694	chr10:49421597-49421598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs546830850	chr10:49421619-49421620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552356145	chr10:49421663-49421664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192365264	chr10:49421668-49421669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs538319143	chr10:49421675-49421676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571254114	chr10:49421686-49421687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562654154	chr10:49421687-49421688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs139900883	chr10:49421698-49421699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs74950624	chr10:49421705-49421706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184785069	chr10:49421749-49421750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs7915014	chr10:49421772-49421773	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs573664966	chr10:49421896-49421897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573053410	chr10:49421899-49421900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533996614	chr10:49421931-49421932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558428573	chr10:49421964-49421965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs578061048	chr10:49421978-49421979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs372931777	chr10:49422000-49422001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542377756	chr10:49422008-49422009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563420065	chr10:49422032-49422033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143323510	chr10:49422071-49422072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575275581	chr10:49422103-49422104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542608877	chr10:49422106-49422107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561248178	chr10:49422107-49422108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs142878669	chr10:49422118-49422119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs111734255	chr10:49422128-49422129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs555706858	chr10:49422240-49422241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532715319	chr10:49422242-49422243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550727548	chr10:49422257-49422258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369849158	chr10:49422311-49422312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575826694	chr10:49422313-49422314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139698407	chr10:49422356-49422357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189820639	chr10:49422434-49422435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548163097	chr10:49422468-49422469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs114839138	chr10:49422480-49422481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533812636	chr10:49422485-49422486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Schizophrenia	23813976	CNVD
Acute myeloid leukemia	19651601	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Rett syndrome	21593744	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
T-cell primary immunodeficiency	21948486	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49415200-49423800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr10:49417200-49432000	Weak transcription	Right Atrium	heart
3	chr10:49418000-49421200	Weak transcription	Brain Angular Gyrus	brain
4	chr10:49419800-49423200	Weak transcription	Fetal Brain Male	brain
5	chr10:49420400-49421200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr10:49420800-49421400	Enhancers	Brain Anterior Caudate	brain
7	chr10:49420800-49421800	Enhancers	Brain Substantia Nigra	brain
8	chr10:49421000-49421400	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr10:49421000-49421400	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr10:49421000-49421400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr10:49421000-49421800	Enhancers	Brain Cingulate Gyrus	brain
12	chr10:49421000-49422200	Enhancers	Brain Hippocampus Middle	brain
13	chr10:49421200-49421400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr10:49421200-49421600	Enhancers	Brain Angular Gyrus	brain
15	chr10:49421400-49422800	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr10:49421400-49423200	Weak transcription	Brain Anterior Caudate	brain
17	chr10:49421600-49422800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr10:49421800-49423400	Weak transcription	Brain Substantia Nigra	brain
19	chr10:49422800-49423200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr10:49422800-49423400	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr10:49423200-49423600	Enhancers	Brain Anterior Caudate	brain
22	chr10:49423200-49423600	Enhancers	Fetal Brain Male	brain
23	chr10:49423200-49423600	Enhancers	GM12878-XiMat	blood
24	chr10:49423400-49423600	Enhancers	Brain Substantia Nigra	brain
25	chr10:49423600-49426400	Weak transcription	Brain Anterior Caudate	brain
26	chr10:49423800-49424400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr10:49423800-49424800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr10:49423800-49424800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr10:49423800-49424800	Enhancers	NHEK	skin
30	chr10:49423800-49425000	Enhancers	HMEC	breast
31	chr10:49423800-49426200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr10:49426200-49430800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr10:49426400-49426800	Strong transcription	Brain Anterior Caudate	brain
34	chr10:49426800-49430400	Weak transcription	Brain Anterior Caudate	brain
35	chr10:49430000-49431000	Weak transcription	Brain Substantia Nigra	brain
36	chr10:49430400-49431600	Strong transcription	Brain Anterior Caudate	brain
37	chr10:49430800-49435000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr10:49431000-49431400	Enhancers	Brain Substantia Nigra	brain
39	chr10:49431400-49433800	Weak transcription	Brain Substantia Nigra	brain
40	chr10:49431600-49441400	Weak transcription	Brain Anterior Caudate	brain
41	chr10:49432000-49434000	Enhancers	Right Atrium	heart
42	chr10:49432200-49432400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr10:49432400-49434200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr10:49432600-49433400	Enhancers	Hela-S3	cervix
45	chr10:49432800-49433000	Enhancers	GM12878-XiMat	blood
46	chr10:49433000-49433400	Enhancers	Pancreas	Pancrea
47	chr10:49433000-49433400	Bivalent Enhancer	HSMMtube	muscle
48	chr10:49433000-49433800	Enhancers	Fetal Heart	heart
49	chr10:49433000-49433800	Enhancers	Osteobl	bone
50	chr10:49433200-49433600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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