Variant report

Variant	nsv437654
Chromosome Location	chr10:4428563-4459527
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:162)
CpG islands
(count:244)
Chromatin interactive
region (count:10)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:162 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr10:4450063-4450365	K562	blood:	n/a	n/a
2	ATF3	chr10:4450065-4450305	K562	blood:	n/a	n/a
3	CCNT2	chr10:4445245-4445354	K562	blood:	n/a	n/a
4	CEBPB	chr10:4439012-4439289	A549	lung:	n/a	chr10:4439203-4439214
5	CEBPB	chr10:4450038-4450415	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr10:4439133-4439333	HepG2	liver:	n/a	chr10:4439203-4439214
7	CEBPB	chr10:4450095-4450387	A549	lung:	n/a	n/a
8	CEBPB	chr10:4454982-4455081	A549	lung:	n/a	chr10:4455002-4455015 chr10:4455004-4455015 chr10:4455002-4455015 chr10:4455002-4455015
9	CEBPB	chr10:4450035-4450513	IMR90	lung:	n/a	n/a
10	CEBPB	chr10:4449931-4450494	HCT-116	colon:	n/a	n/a
11	CEBPB	chr10:4450146-4450358	K562	blood:	n/a	n/a
12	CEBPB	chr10:4450009-4450498	HCT-116	colon:	n/a	n/a
13	CEBPB	chr10:4450102-4450319	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr10:4434000-4434150	HPF	lung:	n/a	n/a
15	CTCF	chr10:4434000-4434150	HCT-116	colon:	n/a	n/a
16	CTCF	chr10:4458520-4458670	GM12872	blood:	n/a	n/a
17	CTCF	chr10:4433984-4434082	Kidney_OC	kidney:	n/a	n/a
18	CTCF	chr10:4433960-4434110	HCM	heart:	n/a	n/a
19	CTCF	chr10:4449265-4449324	ProgFib	skin:	n/a	n/a
20	CTCF	chr10:4433960-4434110	HMEC	breast:	n/a	n/a
21	CTCF	chr10:4433940-4434090	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr10:4433960-4434110	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr10:4433960-4434110	WERI-Rb-1	eye:	n/a	n/a
24	CTCF	chr10:4433940-4434090	Caco-2	colon:	n/a	n/a
25	CTCF	chr10:4433980-4434130	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr10:4431835-4431898	MCF-7	breast:	n/a	n/a
27	CTCF	chr10:4433985-4434125	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr10:4433920-4434070	HFF	foreskin:	n/a	n/a
29	CTCF	chr10:4433943-4434149	ProgFib	skin:	n/a	n/a
30	CTCF	chr10:4433962-4434153	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr10:4433920-4434070	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr10:4433980-4434130	Caco-2	colon:	n/a	n/a
33	CTCF	chr10:4433979-4434169	A549	lung:	n/a	n/a
34	CTCF	chr10:4433960-4434110	HRE	kidney:	n/a	n/a
35	CTCF	chr10:4433980-4434130	HCT-116	colon:	n/a	n/a
36	CTCF	chr10:4434020-4434170	AG09309	skin:	n/a	n/a
37	CTCF	chr10:4446140-4446166	MCF-7	breast:	n/a	n/a
38	CTCF	chr10:4433827-4434234	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr10:4433980-4434130	GM12873	blood:	n/a	n/a
40	CTCF	chr10:4433900-4434050	GM06990	blood:	n/a	n/a
41	CTCF	chr10:4433973-4434150	A549	lung:	n/a	n/a
42	CTCF	chr10:4433940-4434090	WI-38	lung:	n/a	n/a
43	CTCF	chr10:4433980-4434130	HEK293	kidney:	n/a	n/a
44	CTCF	chr10:4433940-4434090	HCFaa	heart:	n/a	n/a
45	CTCF	chr10:4434100-4434250	HVMF	connective:	n/a	n/a
46	CTCF	chr10:4433960-4434110	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr10:4434060-4434210	GM12872	blood:	n/a	n/a
48	CTCF	chr10:4433940-4434090	HMEC	breast:	n/a	n/a
49	CTCF	chr10:4433980-4434130	HVMF	connective:	n/a	n/a
50	CTCF	chr10:4433960-4434110	NB4	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:4446264-4446314	Hela-S3	cervix:	n/a
2	chr10:4446264-4446314	BJ	skin:	n/a
3	chr10:4445958-4446008	ovcar-3	ovarian:	n/a
4	chr10:4446264-4446314	NB4	blood:	n/a
5	chr10:4445948-4445998	GM19239	blood:	n/a
6	chr10:4445948-4445998	MCF10A-Er-Src	breast:	n/a
7	chr10:4445958-4446008	HCF	heart:	n/a
8	chr10:4445958-4446008	HEK293	kidney:	embryo
9	chr10:4445958-4446008	HRE	kidney:	n/a
10	chr10:4446152-4446202	SK-N-SH_RA	brain:	n/a
11	chr10:4446264-4446314	SKMC	muscle:	n/a
12	chr10:4446152-4446202	HEK293	kidney:	embryo
13	chr10:4445958-4446008	GM12891	blood:	n/a
14	chr10:4445948-4445998	NT2-D1	testis:	n/a
15	chr10:4445958-4446008	AG10803	skin:	n/a
16	chr10:4446264-4446314	HRCEpiC	kidney:	n/a
17	chr10:4445948-4445998	BE2_C	brain:	n/a
18	chr10:4446264-4446314	Jurkat	blood:	n/a
19	chr10:4445948-4445998	HMEC	breast:	n/a
20	chr10:4446264-4446314	CMK	blood:	n/a
21	chr10:4445958-4446008	HNPCEpiC	eye:	n/a
22	chr10:4446264-4446314	A549	lung:	n/a
23	chr10:4446152-4446202	HRCEpiC	kidney:	n/a
24	chr10:4445958-4446008	U87	brain:	n/a
25	chr10:4445958-4446008	AoSMC	blood vessel:	n/a
26	chr10:4446264-4446314	HCM	heart:	n/a
27	chr10:4446264-4446314	IMR90	lung:	fetal
28	chr10:4445948-4445998	HRPEpiC	eye:	n/a
29	chr10:4445948-4445998	GM06990	blood:	n/a
30	chr10:4446264-4446314	HPAEpiC	pulmonary alveolar:	n/a
31	chr10:4445948-4445998	MCF-7	breast:	n/a
32	chr10:4446152-4446202	IMR90	lung:	fetal
33	chr10:4445958-4446008	MCF10A-Er-Src	breast:	n/a
34	chr10:4445948-4445998	HUVEC	blood vessel:	n/a
35	chr10:4445948-4445998	AG09319	gingival:	n/a
36	chr10:4446152-4446202	HIPEpiC	eye:	n/a
37	chr10:4446264-4446314	H1-hESC	embryonic stem cell:	embryo
38	chr10:4445958-4446008	HCM	heart:	n/a
39	chr10:4446264-4446314	PANC-1	pancreas:	n/a
40	chr10:4446152-4446202	LNCaP	prostate:	n/a
41	chr10:4445948-4445998	PFSK-1	brain:	n/a
42	chr10:4446152-4446202	HRE	kidney:	n/a
43	chr10:4445948-4445998	K562	blood:	n/a
44	chr10:4445958-4446008	HRCEpiC	kidney:	n/a
45	chr10:4445948-4445998	HL-60	blood:	n/a
46	chr10:4445958-4446008	SK-N-SH_RA	brain:	n/a
47	chr10:4445958-4446008	HMEC	breast:	n/a
48	chr10:4445958-4446008	Jurkat	blood:	n/a
49	chr10:4445958-4446008	NH-A	brain:	n/a
50	chr10:4445948-4445998	GM12891	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:4444626..4446965-chr10:4448966..4451413,2	MCF-7	breast:
2	chr10:4434676..4437518-chr10:4437694..4440629,2	K562	blood:
3	chr10:4450332..4452001-chr10:4468987..4471359,2	MCF-7	breast:
4	chr10:4416065..4417735-chr10:4428097..4429732,2	MCF-7	breast:
5	chr10:4439896..4442775-chr10:4444493..4446676,3	K562	blood:
6	chr10:4426257..4428448-chr10:4431344..4433633,2	K562	blood:
7	chr10:4445300..4447250-chr10:4448228..4450921,2	MCF-7	breast:
8	chr10:4439896..4442775-chr10:4444493..4446676,3	K562	blood:
9	chr10:4434676..4437518-chr10:4437694..4440629,2	K562	blood:
10	chr10:4444626..4446965-chr10:4448966..4451413,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKR1E2-9	chr10:4440647-4440996	l_242_chr10:4438632-4440996_testes
2	lnc-KLF6-15	chr10:4438317-4438544	l_241_chr10:4417616-4438544_testes
3	lnc-AKR1E2-2	chr10:4448694-4448765	XLOC_008361
4	lnc-AKR1E2-2	chr10:4450647-4451443	XLOC_008361
5	lnc-AKR1E2-2	chr10:4450647-4452804	NR_108056
6	lnc-AKR1C2-10	chr10:4433824-4434147	NONHSAT011092
7	lnc-AKR1E2-2	chr10:4433916-4434018	NR_108054
8	lnc-AKR1E2-9	chr10:4438694-4438765	NONHSAT011093
9	lnc-AKR1E2-2	chr10:4450647-4450858	NONHSAT011095
10	lnc-AKR1C2-5	chr10:4458461-4458669	XLOC_008702
11	lnc-AKR1E2-2	chr10:4450647-4452804	NR_108054
12	lnc-AKR1E2-2	chr10:4448665-4448765	NONHSAT011095
13	lnc-AKR1C2-10	chr10:4447497-4447727	NONHSAT011094
14	lnc-AKR1E2-9	chr10:4440647-4441443	NONHSAT011093
15	lnc-AKR1C2-10	chr10:4455742-4455883	NONHSAT011094
16	lnc-KLF6-15	chr10:4436601-4436808	l_241_chr10:4417616-4438544_testes
17	lnc-AKR1C2-10	chr10:4458263-4458371	NONHSAT011094
18	lnc-AKR1C2-5	chr10:4457497-4457727	XLOC_008702
19	lnc-AKR1C2-10	chr10:4448317-4448529	NONHSAT011092
20	lnc-AKR1E2-9	chr10:4440647-4442804	NONHSAT011090
21	lnc-AKR1E2-2	chr10:4448661-4448765	NR_108056
22	lnc-AKR1E2-2	chr10:4458788-4458809	NONHSAT011095
23	lnc-AKR1E2-2	chr10:4450647-4452804	XLOC_008361
24	lnc-AKR1E2-9	chr10:4438633-4438765	l_242_chr10:4438632-4440996_testes
25	lnc-AKR1C2-10	chr10:4448461-4448669	NONHSAT011094

No data

Variant related genes	Relation type
LINC00703	TF binding region
LINC00703	CpG island
ENSG00000224382	chromatin interactions
USP46	miRNA target sites
USP47	miRNA target sites

Extended variants
information (count: 1001 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1001 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534459664	chr10:4431392-4431393	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs141986251	chr10:4431393-4431394	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs147841432	chr10:4431412-4431413	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs368019583	chr10:4431416-4431417	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs575520364	chr10:4431423-4431424	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs1751312	chr10:4431428-4431429	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs71477854	chr10:4431436-4431437	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs202203711	chr10:4431441-4431442	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs35412042	chr10:4431448-4431449	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs563456394	chr10:4431451-4431452	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs575363064	chr10:4431477-4431478	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs73592793	chr10:4431479-4431480	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs77800788	chr10:4431491-4431492	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs138245446	chr10:4431511-4431512	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs547150481	chr10:4431594-4431595	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs1952231	chr10:4431610-4431611	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs529290621	chr10:4431621-4431622	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs186329521	chr10:4431645-4431646	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs192071324	chr10:4431656-4431657	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs539972873	chr10:4431704-4431705	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs1679448	chr10:4431716-4431717	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs544472843	chr10:4431733-4431734	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs534401578	chr10:4431748-4431749	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs1679449	chr10:4431762-4431763	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs183965250	chr10:4431769-4431770	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs74113206	chr10:4431770-4431771	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs557180782	chr10:4431771-4431772	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs144266444	chr10:4431785-4431786	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs114293131	chr10:4431804-4431805	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs557969302	chr10:4431832-4431833	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs549406966	chr10:4431853-4431854	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs112622720	chr10:4431854-4431855	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs112606035	chr10:4431858-4431859	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs529245176	chr10:4431859-4431860	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs544281377	chr10:4431877-4431878	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs114762359	chr10:4431899-4431900	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs72766495	chr10:4431904-4431905	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs375423150	chr10:4431908-4431909	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs551694193	chr10:4431923-4431924	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs368302167	chr10:4431955-4431956	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs555665676	chr10:4431983-4431984	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs555057865	chr10:4431989-4431990	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs372221863	chr10:4431990-4431991	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs186135883	chr10:4431995-4431996	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs538031440	chr10:4432005-4432006	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs377339288	chr10:4432133-4432134	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs143173023	chr10:4432135-4432136	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs147544436	chr10:4432136-4432137	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs556673443	chr10:4432138-4432139	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs140165728	chr10:4432161-4432162	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	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
Breast cancer	21611746	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4433600-4434000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr10:4433800-4434400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr10:4433800-4434400	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr10:4434000-4434400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr10:4437600-4438600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr10:4438600-4441600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr10:4438800-4440200	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr10:4441400-4442400	Enhancers	HSMMtube	muscle
9	chr10:4441600-4442000	Enhancers	Fetal Heart	heart
10	chr10:4441600-4442200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr10:4441600-4442400	Enhancers	Muscle Satellite Cultured Cells	--
12	chr10:4441600-4442400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr10:4441800-4442200	Enhancers	HSMM	muscle
14	chr10:4442000-4442200	Enhancers	NHDF-Ad	bronchial
15	chr10:4442000-4442400	Enhancers	Fetal Brain Male	brain
16	chr10:4442200-4450000	Weak transcription	NHDF-Ad	bronchial
17	chr10:4447400-4447600	Enhancers	Fetal Lung	lung
18	chr10:4448000-4448400	Enhancers	Colon Smooth Muscle	Colon
19	chr10:4448000-4448800	Enhancers	Fetal Heart	heart
20	chr10:4448200-4448400	Enhancers	Fetal Lung	lung
21	chr10:4448400-4448600	Enhancers	NHLF	lung
22	chr10:4448400-4451000	Weak transcription	Colon Smooth Muscle	Colon
23	chr10:4448800-4451000	Weak transcription	Fetal Heart	heart
24	chr10:4449000-4454200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr10:4449200-4451800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr10:4449600-4451600	Enhancers	Muscle Satellite Cultured Cells	--
27	chr10:4449800-4450800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr10:4449800-4450800	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr10:4449800-4450800	Enhancers	HMEC	breast
30	chr10:4449800-4451000	Enhancers	Dnd41	blood
31	chr10:4449800-4451000	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr10:4449800-4451000	Enhancers	NHEK	skin
33	chr10:4449800-4451000	Enhancers	Osteobl	bone
34	chr10:4449800-4451200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr10:4450000-4450400	Enhancers	Hela-S3	cervix
36	chr10:4450000-4450800	Enhancers	HUVEC	blood vessel
37	chr10:4450000-4451000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr10:4450000-4451000	Enhancers	NHDF-Ad	bronchial
39	chr10:4450200-4450800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr10:4450200-4450800	Enhancers	NHLF	lung
41	chr10:4450200-4451000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr10:4450400-4450800	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr10:4450600-4452000	Enhancers	Aorta	Aorta
44	chr10:4450800-4451800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr10:4451000-4452000	Enhancers	Colon Smooth Muscle	Colon
46	chr10:4451000-4452000	Enhancers	Fetal Heart	heart
47	chr10:4451200-4452000	Enhancers	Left Ventricle	heart
48	chr10:4451200-4452000	Enhancers	Rectal Smooth Muscle	rectum
49	chr10:4451800-4452200	Enhancers	Right Atrium	heart
50	chr10:4451800-4452200	Enhancers	Stomach Smooth Muscle	stomach

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