Variant report

Variant	nsv528504
Chromosome Location	chr10:5739054-5754611
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5739648-5740302	K562	blood:	n/a	n/a
2	BACH1	chr10:5746580-5746627	K562	blood:	n/a	n/a
3	CEBPB	chr10:5739870-5740070	IMR90	lung:	n/a	chr10:5739960-5739971
4	CEBPB	chr10:5741244-5741494	A549	lung:	n/a	chr10:5741366-5741377
5	CEBPB	chr10:5741192-5741515	K562	blood:	n/a	chr10:5741366-5741377
6	CEBPB	chr10:5741198-5741547	K562	blood:	n/a	chr10:5741366-5741377
7	CEBPB	chr10:5741245-5741471	H1-hESC	embryonic stem cell:	n/a	chr10:5741366-5741377
8	CEBPB	chr10:5739796-5740140	K562	blood:	n/a	chr10:5739960-5739971
9	CEBPB	chr10:5739840-5740127	HepG2	liver:	n/a	chr10:5739960-5739971
10	CEBPB	chr10:5741239-5741541	IMR90	lung:	n/a	chr10:5741366-5741377
11	CEBPB	chr10:5741255-5741460	HepG2	liver:	n/a	chr10:5741366-5741377
12	CHD1	chr10:5753181-5753222	GM12878	blood:	n/a	n/a
13	CTCF	chr10:5747000-5747150	HPAF	blood vessel:	n/a	n/a
14	CTCF	chr10:5743366-5743406	LNCaP	prostate:	n/a	n/a
15	CTCF	chr10:5748400-5748422	K562	blood:	n/a	n/a
16	CUX1	chr10:5739955-5740155	K562	blood:	n/a	n/a
17	CUX1	chr10:5746938-5746999	GM12878	blood:	n/a	n/a
18	CUX1	chr10:5745078-5745219	GM12878	blood:	n/a	n/a
19	EBF1	chr10:5753520-5753903	GM12878	blood:	n/a	chr10:5753650-5753661
20	EP300	chr10:5739415-5739699	K562	blood:	n/a	n/a
21	GATA1	chr10:5739315-5740745	PBDE	blood:	n/a	chr10:5739624-5739645 chr10:5739631-5739638
22	GATA2	chr10:5740023-5740420	SH-SY5Y	brain:	n/a	n/a
23	GATA2	chr10:5739368-5739763	SH-SY5Y	brain:	n/a	chr10:5739624-5739645 chr10:5739631-5739638
24	GATA3	chr10:5739465-5739789	SH-SY5Y	brain:	n/a	chr10:5739624-5739645 chr10:5739631-5739638
25	GATA3	chr10:5752224-5752351	SH-SY5Y	brain:	n/a	n/a
26	GATA3	chr10:5740051-5740557	SH-SY5Y	brain:	n/a	n/a
27	GATA3	chr10:5743042-5743511	SH-SY5Y	brain:	n/a	n/a
28	IRF1	chr10:5752750-5753186	K562	blood:	n/a	chr10:5753014-5753028 chr10:5753011-5753025 chr10:5753033-5753047 chr10:5753013-5753027 chr10:5753013-5753026 chr10:5753027-5753041 chr10:5753015-5753029 chr10:5753012-5753026 chr10:5753037-5753048 chr10:5753015-5753025 chr10:5753016-5753027 chr10:5753013-5753026 chr10:5753030-5753047 chr10:5753012-5753029 chr10:5753014-5753031 chr10:5752762-5752769 chr10:5753013-5753026 chr10:5753030-5753042 chr10:5753015-5753026 chr10:5753036-5753048
29	IRF1	chr10:5752840-5753117	K562	blood:	n/a	chr10:5753014-5753028 chr10:5753011-5753025 chr10:5753033-5753047 chr10:5753013-5753027 chr10:5753013-5753026 chr10:5753027-5753041 chr10:5753015-5753029 chr10:5753012-5753026 chr10:5753037-5753048 chr10:5753015-5753025 chr10:5753016-5753027 chr10:5753013-5753026 chr10:5753030-5753047 chr10:5753012-5753029 chr10:5753014-5753031 chr10:5753013-5753026 chr10:5753030-5753042 chr10:5753015-5753026 chr10:5753036-5753048
30	IRF1	chr10:5740134-5740332	K562	blood:	n/a	n/a
31	JUN	chr10:5754001-5754021	H1-hESC	embryonic stem cell:	n/a	n/a
32	JUND	chr10:5739555-5739696	K562	blood:	n/a	n/a
33	KAP1	chr10:5739280-5739804	HEK293	kidney:	n/a	n/a
34	MAZ	chr10:5739485-5739722	K562	blood:	n/a	n/a
35	MAZ	chr10:5739157-5739199	K562	blood:	n/a	n/a
36	MYC	chr10:5753535-5753713	MCF10A-Er-Src	breast:	n/a	n/a
37	NFYA	chr10:5748190-5748210	GM12878	blood:	n/a	n/a
38	NFYB	chr10:5740148-5740365	K562	blood:	n/a	n/a
39	NFYB	chr10:5740042-5740265	GM12878	blood:	n/a	n/a
40	POLR2A	chr10:5749733-5749836	MCF-7	breast:	n/a	n/a
41	POLR2A	chr10:5741429-5741538	K562	blood:	n/a	n/a
42	POLR2A	chr10:5739514-5739714	HepG2	liver:	n/a	n/a
43	POLR2A	chr10:5748758-5748764	GM12878	blood:	n/a	n/a
44	POLR2A	chr10:5741739-5742158	K562	blood:	n/a	n/a
45	POLR2A	chr10:5739357-5739433	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr10:5746978-5747152	MCF10A-Er-Src	breast:	n/a	n/a
47	RCOR1	chr10:5739450-5739763	K562	blood:	n/a	n/a
48	RUNX3	chr10:5740292-5740693	GM12878	blood:	n/a	chr10:5740426-5740435 chr10:5740426-5740435
49	RUNX3	chr10:5746794-5747091	GM12878	blood:	n/a	n/a
50	STAT3	chr10:5750968-5751047	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:5733360..5736300-chr10:5737628..5741126,5	MCF-7	breast:
2	chr10:5732181..5739053-chr10:5741617..5746199,6	MCF-7	breast:
3	chr10:5726042..5728288-chr10:5749073..5750602,2	MCF-7	breast:
4	chr10:5725582..5728827-chr10:5752793..5758658,6	MCF-7	breast:
5	chr10:5706900..5709374-chr10:5740250..5741979,2	MCF-7	breast:
6	chr10:5734698..5736593-chr10:5746537..5749432,2	MCF-7	breast:
7	chr10:5748194..5752835-chr10:5754048..5756817,4	MCF-7	breast:
8	chr10:5726410..5728417-chr10:5738015..5741917,3	MCF-7	breast:
9	chr10:5724274..5728540-chr10:5734829..5741563,8	MCF-7	breast:
10	chr10:5487728..5489402-chr10:5743832..5746682,2	MCF-7	breast:
11	chr10:5726626..5728206-chr10:5753168..5755087,2	K562	blood:
12	chr10:5751112..5753798-chr10:5754382..5757716,3	K562	blood:
13	chr10:5729840..5732495-chr10:5739235..5741106,2	MCF-7	breast:
14	chr10:5749331..5751583-chr10:5752146..5753784,2	MCF-7	breast:
15	chr10:5747573..5749286-chr10:5752510..5754353,2	K562	blood:
16	chr10:5725406..5728715-chr10:5747568..5751515,5	MCF-7	breast:
17	chr10:5585750..5587884-chr10:5738818..5740542,2	K562	blood:
18	chr10:5748219..5750363-chr10:5854486..5857836,3	K562	blood:
19	chr10:5739796..5741781-chr10:5749171..5751664,2	K562	blood:
20	chr10:5751112..5753798-chr10:5754382..5757716,3	K562	blood:
21	chr10:5748194..5752835-chr10:5754048..5756817,4	MCF-7	breast:
22	chr10:5733787..5736575-chr10:5751182..5753712,2	MCF-7	breast:
23	chr10:5734758..5736346-chr10:5739333..5741720,2	MCF-7	breast:
24	chr10:5737326..5739856-chr10:5853864..5856173,2	MCF-7	breast:
25	chr10:5733731..5736743-chr10:5750015..5755601,4	MCF-7	breast:
26	chr10:5747573..5749286-chr10:5752510..5754353,2	K562	blood:
27	chr10:5749331..5751583-chr10:5752146..5753784,2	MCF-7	breast:
28	chr10:5739796..5741781-chr10:5749171..5751664,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GDI2-1	chr10:5754383-5754651	ENSG00000226647.2
2	lnc-CALML3-1	chr10:5751493-5751626	NONHSAT011176
3	lnc-CALML3-1	chr10:5741411-5741700	NONHSAT011177
4	lnc-CALML3-1	chr10:5751493-5751626	NONHSAT011177
5	lnc-GDI2-1	chr10:5754137-5754651	ENSG00000226647.2
6	lnc-CALML3-1	chr10:5754357-5754502	NONHSAT011176
7	lnc-GDI2-1	chr10:5754177-5754651	ENSG00000226647.1

Variant related genes	Relation type
FAM208B	TF binding region
ENSG00000057608	chromatin interactions
ENSG00000108021	chromatin interactions
ENSG00000196372	chromatin interactions
ENSG00000272764	chromatin interactions
ENSG00000173848	chromatin interactions
ENSG00000226647	chromatin interactions

Extended variants
information (count: 550 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7908235	chr10:5739054-5739055	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs543101812	chr10:5739063-5739064	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs143404951	chr10:5739073-5739074	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs190949060	chr10:5739074-5739075	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs550459442	chr10:5739080-5739081	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs563690518	chr10:5739111-5739112	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs568825343	chr10:5739132-5739133	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs181414149	chr10:5739177-5739178	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs550990083	chr10:5739191-5739192	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs566114809	chr10:5739203-5739204	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs373858120	chr10:5739233-5739234	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs61832742	chr10:5739254-5739255	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs200955990	chr10:5739255-5739256	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs35615005	chr10:5739256-5739257	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs72507172	chr10:5739257-5739258	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs397756822	chr10:5739258-5739259	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs79594128	chr10:5739259-5739260	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs139377112	chr10:5739297-5739298	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs531203676	chr10:5739326-5739327	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs186491036	chr10:5739336-5739337	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs556453520	chr10:5739337-5739338	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs578257196	chr10:5739339-5739340	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs545703269	chr10:5739355-5739356	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs554250458	chr10:5739400-5739401	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs191767774	chr10:5739413-5739414	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs143192242	chr10:5739414-5739415	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs183045748	chr10:5739497-5739498	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs561440720	chr10:5739498-5739499	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs552932327	chr10:5739502-5739503	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs147099155	chr10:5739529-5739530	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs138010825	chr10:5739547-5739548	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs187377250	chr10:5739594-5739595	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs533091304	chr10:5739702-5739703	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs551252206	chr10:5739792-5739793	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs566177618	chr10:5739801-5739802	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs191088128	chr10:5739829-5739830	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs548668215	chr10:5739842-5739843	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs567377300	chr10:5739849-5739850	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs11817140	chr10:5739862-5739863	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs537522548	chr10:5739871-5739872	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs571044838	chr10:5739874-5739875	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs143529582	chr10:5739893-5739894	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs571861714	chr10:5739936-5739937	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs539389743	chr10:5739985-5739986	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs566628012	chr10:5740073-5740074	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs183272559	chr10:5740082-5740083	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs572734432	chr10:5740146-5740147	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs536661576	chr10:5740235-5740236	Enhancers Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs528727942	chr10:5740254-5740255	Enhancers Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs568139259	chr10:5740256-5740257	Enhancers Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
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
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Ovarian cancer	22355333	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:449 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5728800-5746800	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr10:5734800-5763400	Weak transcription	HSMM	muscle
3	chr10:5735200-5739400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr10:5735200-5739400	Weak transcription	Lung	lung
5	chr10:5735200-5739400	Weak transcription	Pancreas	Pancrea
6	chr10:5735200-5739800	Enhancers	Primary T killer memory cells from peripheral blood	blood
7	chr10:5735200-5743000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr10:5735200-5749000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr10:5735200-5750600	Weak transcription	Gastric	stomach
10	chr10:5735200-5767000	Weak transcription	Fetal Muscle Leg	muscle
11	chr10:5735400-5739200	Weak transcription	Fetal Heart	heart
12	chr10:5735400-5739200	Weak transcription	Fetal Intestine Small	intestine
13	chr10:5735400-5739400	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr10:5735400-5739400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr10:5735400-5739400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr10:5735400-5739600	Weak transcription	Colonic Mucosa	Colon
17	chr10:5735400-5744800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr10:5735400-5750800	Weak transcription	Spleen	Spleen
19	chr10:5735400-5761600	Weak transcription	NHEK	skin
20	chr10:5735400-5762000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr10:5735800-5741800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr10:5735800-5752800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr10:5736000-5739600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr10:5736200-5739200	Weak transcription	Thymus	Thymus
25	chr10:5736200-5739400	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr10:5736200-5739600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr10:5736200-5740000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr10:5736200-5740200	Weak transcription	A549	lung
29	chr10:5736200-5742600	Weak transcription	Brain Angular Gyrus	brain
30	chr10:5736200-5751600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr10:5736400-5739200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr10:5736400-5741000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr10:5736400-5753000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr10:5736600-5741600	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr10:5736800-5739400	Weak transcription	Primary B cells from peripheral blood	blood
36	chr10:5736800-5742000	Weak transcription	Primary T cells from cord blood	blood
37	chr10:5736800-5742000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr10:5737000-5739200	Weak transcription	Stomach Mucosa	stomach
39	chr10:5737000-5742000	Weak transcription	Brain Substantia Nigra	brain
40	chr10:5737000-5742600	Weak transcription	Brain Hippocampus Middle	brain
41	chr10:5737000-5743600	Weak transcription	Primary hematopoietic stem cells	blood
42	chr10:5737400-5739400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr10:5737400-5744200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr10:5737400-5744800	Weak transcription	Liver	Liver
45	chr10:5737600-5740200	Enhancers	HepG2	liver
46	chr10:5737600-5740800	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr10:5737600-5744200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr10:5737800-5739200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr10:5738000-5740600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr10:5738000-5740600	Enhancers	HUES6 Cell Line	embryonic stem cell

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