Variant report

Variant	nsv1047686
Chromosome Location	chr10:5148453-5185582
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:165)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:165 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr10:5149405-5152719	A549	lung:	n/a	chr10:5151173-5151180 chr10:5151748-5151757
2	BCL3	chr10:5149846-5152451	A549	lung:	n/a	chr10:5151173-5151180 chr10:5151748-5151757
3	BHLHE40	chr10:5185410-5185563	HepG2	liver:	n/a	n/a
4	CBX3	chr10:5178725-5179069	K562	blood:	n/a	n/a
5	CBX3	chr10:5178706-5179040	HCT-116	colon:	n/a	n/a
6	CBX3	chr10:5178698-5179012	K562	blood:	n/a	n/a
7	CEBPB	chr10:5167486-5167892	MCF-7	breast:	n/a	n/a
8	CEBPB	chr10:5167523-5167909	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr10:5167491-5167948	MCF-7	breast:	n/a	n/a
10	CEBPB	chr10:5185573-5185765	HepG2	liver:	n/a	n/a
11	CHD2	chr10:5150557-5150566	HepG2	liver:	n/a	n/a
12	CREB1	chr10:5150066-5150344	A549	lung:	n/a	n/a
13	CTCF	chr10:5185080-5185230	HepG2	liver:	n/a	n/a
14	CTCF	chr10:5152476-5152601	MCF-7	breast:	n/a	n/a
15	CTCF	chr10:5165940-5165953	GM20000	blood:	n/a	n/a
16	CTCF	chr10:5152454-5152607	MCF-7	breast:	n/a	n/a
17	CTCF	chr10:5164300-5164336	GM20000	blood:	n/a	n/a
18	CTCF	chr10:5166224-5166285	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr10:5152487-5152584	MCF-7	breast:	n/a	n/a
20	ELF1	chr10:5151219-5151549	A549	lung:	n/a	n/a
21	EP300	chr10:5167537-5167881	Hela-S3	cervix:	n/a	n/a
22	EP300	chr10:5185277-5185722	HepG2	liver:	n/a	n/a
23	EP300	chr10:5160356-5160892	MCF-7	breast:	n/a	n/a
24	ETS1	chr10:5151429-5151957	A549	lung:	n/a	n/a
25	FOS	chr10:5167631-5167831	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr10:5167560-5167873	MCF10A-Er-Src	breast:	n/a	n/a
27	FOSL2	chr10:5149725-5150628	A549	lung:	n/a	chr10:5150441-5150452
28	FOSL2	chr10:5150743-5152099	A549	lung:	n/a	n/a
29	FOXA1	chr10:5152153-5152418	HepG2	liver:	n/a	n/a
30	FOXA1	chr10:5150233-5150579	HepG2	liver:	n/a	n/a
31	FOXA1	chr10:5152183-5152314	T-47D	breast:	n/a	n/a
32	FOXA1	chr10:5160159-5160498	HepG2	liver:	n/a	n/a
33	FOXA1	chr10:5160083-5160511	HepG2	liver:	n/a	n/a
34	FOXA2	chr10:5151898-5152641	A549	lung:	n/a	n/a
35	FOXA2	chr10:5152034-5152581	A549	lung:	n/a	n/a
36	FOXA2	chr10:5150388-5150834	A549	lung:	n/a	n/a
37	FOXA2	chr10:5150353-5150654	A549	lung:	n/a	n/a
38	GATA3	chr10:5160546-5160664	MCF-7	breast:	n/a	n/a
39	GATA3	chr10:5158224-5158483	MCF-7	breast:	n/a	n/a
40	GATA3	chr10:5150184-5152082	A549	lung:	n/a	chr10:5151169-5151185
41	GATA3	chr10:5160197-5160917	MCF-7	breast:	n/a	n/a
42	GATA3	chr10:5158193-5158727	MCF-7	breast:	n/a	n/a
43	GATA3	chr10:5158217-5158664	MCF-7	breast:	n/a	n/a
44	GATA3	chr10:5167495-5167918	MCF-7	breast:	n/a	n/a
45	HDAC2	chr10:5185412-5185661	HepG2	liver:	n/a	n/a
46	HEY1	chr10:5174700-5174995	HepG2	liver:	n/a	n/a
47	HEY1	chr10:5150247-5150558	HepG2	liver:	n/a	n/a
48	HNF4A	chr10:5185311-5185773	HepG2	liver:	n/a	chr10:5185557-5185572
49	HNF4A	chr10:5185260-5185721	HepG2	liver:	n/a	chr10:5185557-5185572
50	HNF4G	chr10:5185175-5185809	HepG2	liver:	n/a	chr10:5185489-5185504

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5149799-5149849	Hepatocyte	liver:	n/a
2	chr10:5149799-5149849	IMR90	lung:	fetal
3	chr10:5149799-5149849	ProgFib	skin:	n/a
4	chr10:5149799-5149849	AG09309	skin:	n/a
5	chr10:5149799-5149849	GM12891	blood:	n/a
6	chr10:5149799-5149849	HRCEpiC	kidney:	n/a
7	chr10:5149799-5149849	Hela-S3	cervix:	n/a
8	chr10:5149799-5149849	HUVEC	blood vessel:	n/a
9	chr10:5149799-5149849	HPAEpiC	pulmonary alveolar:	n/a
10	chr10:5149799-5149849	HIPEpiC	eye:	n/a
11	chr10:5149799-5149849	HRPEpiC	eye:	n/a
12	chr10:5149799-5149849	RPTEC	kidney:	n/a
13	chr10:5149799-5149849	HMEC	breast:	n/a
14	chr10:5149799-5149849	GM12878	blood:	n/a
15	chr10:5149799-5149849	H1-hESC	embryonic stem cell:	embryo
16	chr10:5149799-5149849	BJ	skin:	n/a
17	chr10:5149799-5149849	A549	lung:	n/a
18	chr10:5149799-5149849	HNPCEpiC	eye:	n/a
19	chr10:5149799-5149849	K562	blood:	n/a
20	chr10:5149799-5149849	GM12892	blood:	n/a
21	chr10:5149799-5149849	AoSMC	blood vessel:	n/a
22	chr10:5149799-5149849	Caco-2	colon:	n/a
23	chr10:5149799-5149849	AG04450	lung:	fetal
24	chr10:5149799-5149849	NHBE	bronchial:	n/a
25	chr10:5149799-5149849	T-47D	breast:	n/a
26	chr10:5149799-5149849	HepG2	liver:	n/a
27	chr10:5149799-5149849	GM06990	blood:	n/a
28	chr10:5149799-5149849	HL-60	blood:	n/a
29	chr10:5149799-5149849	SAEC	small airway:	n/a
30	chr10:5149799-5149849	SK-N-SH_RA	brain:	n/a
31	chr10:5149799-5149849	Jurkat	blood:	n/a
32	chr10:5149799-5149849	LNCaP	prostate:	n/a
33	chr10:5149799-5149849	HEEpiC	esophagus:	n/a
34	chr10:5149799-5149849	SKMC	muscle:	n/a
35	chr10:5149799-5149849	GM19239	blood:	n/a
36	chr10:5149799-5149849	HRE	kidney:	n/a
37	chr10:5149799-5149849	MCF-7	breast:	n/a
38	chr10:5149799-5149849	ECC-1	luminal epithelium:	n/a
39	chr10:5149799-5149849	NB4	blood:	n/a
40	chr10:5149799-5149849	PFSK-1	brain:	n/a
41	chr10:5149799-5149849	AG04449	skin:	fetal
42	chr10:5149799-5149849	HEK293	kidney:	embryo
43	chr10:5149799-5149849	PANC-1	pancreas:	n/a
44	chr10:5149799-5149849	SK-N-MC	brain:	n/a
45	chr10:5149799-5149849	ovcar-3	ovarian:	n/a
46	chr10:5149799-5149849	PrEC	prostate:	n/a
47	chr10:5149799-5149849	NH-A	brain:	n/a
48	chr10:5149799-5149849	HCF	heart:	n/a
49	chr10:5149799-5149849	SK-N-SH	brain:	n/a
50	chr10:5149799-5149849	NHDF-neo	bronchial:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:5159415..5162131-chr10:5167591..5169595,2	MCF-7	breast:
2	chr10:5135013..5137947-chr10:5149855..5151840,2	MCF-7	breast:
3	chr10:5149764..5151896-chr10:5189814..5192281,2	MCF-7	breast:
4	chr10:5163399..5166048-chr10:5166871..5170286,3	K562	blood:
5	chr10:5136589..5138613-chr10:5158907..5161668,2	MCF-7	breast:
6	chr10:5171829..5174408-chr10:5176222..5177928,2	MCF-7	breast:
7	chr10:5157749..5160543-chr10:5164093..5166584,2	MCF-7	breast:
8	chr10:5159415..5162131-chr10:5167591..5169595,2	MCF-7	breast:
9	chr10:5140565..5143325-chr10:5148088..5150883,2	MCF-7	breast:
10	chr10:5169411..5171944-chr10:5173509..5175691,2	K562	blood:
11	chr10:5163399..5166048-chr10:5166871..5170286,3	K562	blood:
12	chr10:5169411..5171944-chr10:5173509..5175691,2	K562	blood:
13	chr10:5157749..5160543-chr10:5164093..5166584,2	MCF-7	breast:
14	chr10:5158412..5160412-chr20:46095387..46097285,2	MCF-7	breast:
15	chr10:5140998..5143202-chr10:5149820..5152620,2	K562	blood:
16	chr10:5166174..5167900-chr10:5189108..5191670,2	MCF-7	breast:

No data

Variant related genes	Relation type
AKR1C5P	TF binding region
AKR1C5P	CpG island
ENSG00000225418	chromatin interactions
ENSG00000196139	chromatin interactions
ENSG00000239142	chromatin interactions

Extended variants
information (count: 1880 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1880 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4641368	chr10:5148453-5148454	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs587609344	chr10:5148507-5148508	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs9888075	chr10:5148530-5148531	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs193064918	chr10:5148546-5148547	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs374469123	chr10:5148552-5148553	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs75243804	chr10:5148576-5148577	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs587665623	chr10:5148584-5148585	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs368404436	chr10:5148592-5148593	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs587605285	chr10:5148600-5148601	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs148061459	chr10:5148605-5148606	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141809141	chr10:5148611-5148612	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs77941994	chr10:5148623-5148624	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs587768185	chr10:5148624-5148625	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs587664786	chr10:5148651-5148652	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs78285039	chr10:5148653-5148654	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs587721341	chr10:5148668-5148669	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs4584484	chr10:5148669-5148670	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs4584485	chr10:5148712-5148713	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs587682977	chr10:5148717-5148718	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185587093	chr10:5148719-5148720	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs587645421	chr10:5148739-5148740	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs587708118	chr10:5148740-5148741	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs4264066	chr10:5148766-5148767	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs587638543	chr10:5148804-5148805	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs587718482	chr10:5148815-5148816	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587593622	chr10:5148841-5148842	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188176925	chr10:5148857-5148858	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs587732023	chr10:5148858-5148859	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs9329315	chr10:5148923-5148924	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs146095583	chr10:5148926-5148927	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs61368631	chr10:5148956-5148957	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs72774027	chr10:5148967-5148968	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs587639824	chr10:5148975-5148976	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs587721379	chr10:5148976-5148977	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs148366905	chr10:5149003-5149004	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs587731350	chr10:5149016-5149017	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs587624686	chr10:5149047-5149048	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs140042540	chr10:5149068-5149069	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs67034166	chr10:5149069-5149070	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs386370544	chr10:5149071-5149072	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs10637297	chr10:5149075-5149076	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs370377342	chr10:5149105-5149106	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs373762373	chr10:5149106-5149107	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs34977292	chr10:5149107-5149108	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs558339615	chr10:5149108-5149109	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs386370545	chr10:5149109-5149110	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs72507161	chr10:5149110-5149111	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs10637298	chr10:5149111-5149112	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs587696378	chr10:5149112-5149113	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs587627799	chr10:5149115-5149116	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
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	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:155 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5137200-5149800	Weak transcription	Small Intestine	intestine
2	chr10:5137400-5149400	Weak transcription	HSMM	muscle
3	chr10:5137400-5149600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr10:5137400-5149600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr10:5137400-5149800	Weak transcription	Pancreas	Pancrea
6	chr10:5137400-5151600	Weak transcription	Brain Angular Gyrus	brain
7	chr10:5137400-5151800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr10:5137400-5152000	Weak transcription	Right Ventricle	heart
9	chr10:5137800-5150800	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr10:5138200-5151000	Weak transcription	Osteobl	bone
11	chr10:5138200-5151800	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr10:5138600-5149200	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr10:5138600-5149800	Weak transcription	Rectal Smooth Muscle	rectum
14	chr10:5138600-5150200	Weak transcription	Brain Hippocampus Middle	brain
15	chr10:5138600-5151800	Weak transcription	Stomach Smooth Muscle	stomach
16	chr10:5138800-5151800	Weak transcription	Brain Anterior Caudate	brain
17	chr10:5138800-5151800	Weak transcription	Colonic Mucosa	Colon
18	chr10:5138800-5152000	Weak transcription	Psoas Muscle	Psoas
19	chr10:5139000-5151600	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr10:5140200-5150400	Strong transcription	Duodenum Mucosa	Duodenum
21	chr10:5140800-5148600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr10:5140800-5149800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr10:5145200-5151400	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr10:5145600-5148600	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr10:5146000-5149600	Weak transcription	Thymus	Thymus
26	chr10:5146000-5150000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr10:5146000-5150400	Weak transcription	Fetal Intestine Small	intestine
28	chr10:5146000-5151600	Weak transcription	Hela-S3	cervix
29	chr10:5146000-5151800	Weak transcription	Esophagus	oesophagus
30	chr10:5146000-5157600	Weak transcription	Primary hematopoietic stem cells	blood
31	chr10:5147400-5148600	Genic enhancers	Liver	Liver
32	chr10:5147400-5150200	Strong transcription	Sigmoid Colon	Sigmoid Colon
33	chr10:5147400-5150200	Strong transcription	Skeletal Muscle Female	skeletal muscle
34	chr10:5147800-5148600	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr10:5147800-5148600	Strong transcription	Skeletal Muscle Male	skeletal muscle
36	chr10:5147800-5148600	Strong transcription	Stomach Mucosa	stomach
37	chr10:5147800-5148600	Transcr. at gene 5' and 3'	A549	lung
38	chr10:5147800-5150600	Strong transcription	Aorta	Aorta
39	chr10:5147800-5151400	Strong transcription	Rectal Mucosa Donor 31	rectum
40	chr10:5148000-5148600	Strong transcription	NHDF-Ad	bronchial
41	chr10:5148000-5148800	Strong transcription	Rectal Mucosa Donor 29	rectum
42	chr10:5148000-5150400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr10:5148000-5150400	Strong transcription	HSMMtube	muscle
44	chr10:5148200-5150000	Strong transcription	HepG2	liver
45	chr10:5148200-5150200	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr10:5148200-5150400	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr10:5148400-5148600	Weak transcription	Gastric	stomach
48	chr10:5148400-5149600	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr10:5148400-5151000	Strong transcription	Adipose Nuclei	Adipose
50	chr10:5148400-5151400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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