Variant report

Variant	esv3418576
Chromosome Location	chr10:25295995-25311122
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	chr10:25308511-25308615	K562	blood:	n/a	n/a
2	ARID3A	chr10:25310199-25310226	K562	blood:	n/a	n/a
3	ARID3A	chr10:25305407-25306063	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:25305605-25306157	K562	blood:	n/a	n/a
5	ARID3A	chr10:25305014-25305247	K562	blood:	n/a	n/a
6	ATF2	chr10:25305510-25306529	GM12878	blood:	n/a	n/a
7	ATF3	chr10:25305334-25305668	HepG2	liver:	n/a	chr10:25305505-25305525
8	ATF3	chr10:25305151-25305745	GM12878	blood:	n/a	chr10:25305505-25305525
9	ATF3	chr10:25305345-25306137	A549	lung:	n/a	chr10:25305505-25305525
10	ATF3	chr10:25305336-25305645	H1-hESC	embryonic stem cell:	n/a	chr10:25305505-25305525
11	ATF3	chr10:25305288-25305742	H1-hESC	embryonic stem cell:	n/a	chr10:25305505-25305525
12	ATF3	chr10:25305443-25305563	GM12878	blood:	n/a	chr10:25305505-25305525
13	ATF3	chr10:25305201-25305988	A549	lung:	n/a	chr10:25305505-25305525
14	ATF3	chr10:25305274-25305698	K562	blood:	n/a	chr10:25305505-25305525
15	BACH1	chr10:25307630-25307993	K562	blood:	n/a	n/a
16	BACH1	chr10:25305245-25306096	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL3	chr10:25305356-25306180	A549	lung:	n/a	chr10:25305543-25305552 chr10:25305876-25305889 chr10:25305914-25305927 chr10:25305683-25305692
18	BCL3	chr10:25304934-25306403	A549	lung:	n/a	chr10:25305543-25305552 chr10:25305876-25305889 chr10:25305914-25305927 chr10:25305683-25305692
19	BCLAF1	chr10:25305576-25306282	GM12878	blood:	n/a	chr10:25305876-25305889 chr10:25305914-25305927 chr10:25305683-25305692
20	BHLHE40	chr10:25304891-25306199	K562	blood:	n/a	chr10:25305504-25305513 chr10:25305505-25305514 chr10:25305506-25305515 chr10:25305499-25305520 chr10:25305505-25305514 chr10:25305959-25305975
21	BHLHE40	chr10:25304980-25306434	GM12878	blood:	n/a	chr10:25305504-25305513 chr10:25305505-25305514 chr10:25305506-25305515 chr10:25305499-25305520 chr10:25305505-25305514 chr10:25305959-25305975
22	BHLHE40	chr10:25304904-25306223	HepG2	liver:	n/a	chr10:25305504-25305513 chr10:25305505-25305514 chr10:25305506-25305515 chr10:25305499-25305520 chr10:25305505-25305514 chr10:25305959-25305975
23	BHLHE40	chr10:25305363-25305984	A549	lung:	n/a	chr10:25305504-25305513 chr10:25305505-25305514 chr10:25305506-25305515 chr10:25305499-25305520 chr10:25305505-25305514 chr10:25305959-25305975
24	BHLHE40	chr10:25305374-25305676	HepG2	liver:	n/a	chr10:25305504-25305513 chr10:25305505-25305514 chr10:25305506-25305515 chr10:25305499-25305520 chr10:25305505-25305514
25	BRCA1	chr10:25306011-25306214	GM12878	blood:	n/a	n/a
26	BRCA1	chr10:25305479-25305810	HepG2	liver:	n/a	n/a
27	BRCA1	chr10:25304919-25306334	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr10:25305866-25306375	H1-hESC	embryonic stem cell:	n/a	n/a
29	CBX3	chr10:25304897-25306553	K562	blood:	n/a	n/a
30	CBX3	chr10:25305131-25306183	K562	blood:	n/a	n/a
31	CCNT2	chr10:25305301-25306204	K562	blood:	n/a	n/a
32	CCNT2	chr10:25307047-25307227	K562	blood:	n/a	n/a
33	CEBPB	chr10:25300659-25300795	K562	blood:	n/a	chr10:25300717-25300728
34	CEBPB	chr10:25305597-25306178	K562	blood:	n/a	n/a
35	CEBPB	chr10:25304444-25304630	A549	lung:	n/a	chr10:25304514-25304523 chr10:25304514-25304525
36	CEBPB	chr10:25307220-25307527	HepG2	liver:	n/a	n/a
37	CEBPB	chr10:25305478-25306376	GM12878	blood:	n/a	n/a
38	CEBPB	chr10:25306458-25306461	HepG2	liver:	n/a	n/a
39	CEBPB	chr10:25305603-25305964	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr10:25307206-25307549	K562	blood:	n/a	n/a
41	CEBPB	chr10:25298224-25298376	K562	blood:	n/a	chr10:25298286-25298299
42	CEBPB	chr10:25300602-25300802	IMR90	lung:	n/a	chr10:25300717-25300728
43	CEBPB	chr10:25300646-25300803	HepG2	liver:	n/a	chr10:25300717-25300728
44	CEBPD	chr10:25305429-25306101	K562	blood:	n/a	n/a
45	CEBPD	chr10:25305787-25306050	HepG2	liver:	n/a	n/a
46	CEBPD	chr10:25305421-25306167	HepG2	liver:	n/a	n/a
47	CHD1	chr10:25305573-25306413	GM12878	blood:	n/a	n/a
48	CHD1	chr10:25306041-25306386	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr10:25305017-25305983	GM12878	blood:	n/a	n/a
50	CHD2	chr10:25304891-25306084	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:25305105-25305155	HCF	heart:	n/a
2	chr10:25306365-25306415	HIPEpiC	eye:	n/a
3	chr10:25305382-25305432	HPAEpiC	pulmonary alveolar:	n/a
4	chr10:25305105-25305155	HCF	heart:	n/a
5	chr10:25306365-25306415	HIPEpiC	eye:	n/a
6	chr10:25305382-25305432	HPAEpiC	pulmonary alveolar:	n/a
7	chr10:25305418-25305468	LNCaP	prostate:	n/a
8	chr10:25305175-25305225	HCF	heart:	n/a
9	chr10:25305217-25305267	HRPEpiC	eye:	n/a
10	chr10:25305695-25305745	K562	blood:	n/a
11	chr10:25305418-25305468	HUVEC	blood vessel:	n/a
12	chr10:25305105-25305155	MCF10A-Er-Src	breast:	n/a
13	chr10:25305002-25305052	SAEC	small airway:	n/a
14	chr10:25305217-25305267	NB4	blood:	n/a
15	chr10:25305096-25305146	SAEC	small airway:	n/a
16	chr10:25305391-25305441	NHDF-neo	bronchial:	n/a
17	chr10:25305105-25305155	Jurkat	blood:	n/a
18	chr10:25305695-25305745	MCF-7	breast:	n/a
19	chr10:25305075-25305125	HCF	heart:	n/a
20	chr10:25306365-25306415	T-47D	breast:	n/a
21	chr10:25305695-25305745	BE2_C	brain:	n/a
22	chr10:25305096-25305146	HMEC	breast:	n/a
23	chr10:25305391-25305441	CMK	blood:	n/a
24	chr10:25305175-25305225	GM12892	blood:	n/a
25	chr10:25305175-25305225	BE2_C	brain:	n/a
26	chr10:25306365-25306415	GM12891	blood:	n/a
27	chr10:25305418-25305468	HepG2	liver:	n/a
28	chr10:25305105-25305155	NHBE	bronchial:	n/a
29	chr10:25305002-25305052	AG10803	skin:	n/a
30	chr10:25303159-25303209	HIPEpiC	eye:	n/a
31	chr10:25306365-25306415	NT2-D1	testis:	n/a
32	chr10:25305418-25305468	Jurkat	blood:	n/a
33	chr10:25305175-25305225	ECC-1	luminal epithelium:	n/a
34	chr10:25305078-25305128	AG10803	skin:	n/a
35	chr10:25305391-25305441	HUVEC	blood vessel:	n/a
36	chr10:25305002-25305052	CMK	blood:	n/a
37	chr10:25305002-25305052	BE2_C	brain:	n/a
38	chr10:25305382-25305432	CMK	blood:	n/a
39	chr10:25305418-25305468	Hela-S3	cervix:	n/a
40	chr10:25305217-25305267	HepG2	liver:	n/a
41	chr10:25305217-25305267	HCF	heart:	n/a
42	chr10:25305096-25305146	SK-N-SH	brain:	n/a
43	chr10:25305105-25305155	Caco-2	colon:	n/a
44	chr10:25305175-25305225	HepG2	liver:	n/a
45	chr10:25305105-25305155	HCPEpiC	choroid plexus:	n/a
46	chr10:25305695-25305745	A549	lung:	n/a
47	chr10:25305002-25305052	HMEC	breast:	n/a
48	chr10:25305175-25305225	U87	brain:	n/a
49	chr10:25306365-25306415	ovcar-3	ovarian:	n/a
50	chr10:25305105-25305155	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:25309325..25311704-chr10:25312754..25314813,2	MCF-7	breast:
2	chr10:25307575..25310244-chr10:25349571..25352250,2	MCF-7	breast:
3	chr10:25305336..25306093-chr7:5569046..5569893,2	Hela-S3	cervix:
4	chr10:25310933..25313238-chr10:25417653..25419899,2	K562	blood:
5	chr10:25008982..25015736-chr10:25303520..25307645,9	MCF-7	breast:
6	chr10:25241117..25243872-chr10:25301053..25303469,2	K562	blood:
7	chr10:25305215..25305986-chr8:33370477..33371308,2	HCT-116	colon:
8	chr10:25310470..25312608-chr10:25316004..25319067,3	MCF-7	breast:
9	chr10:25308766..25310925-chr10:25358161..25359867,2	K562	blood:
10	chr10:25306319..25307953-chr10:25346499..25349389,2	MCF-7	breast:
11	chr10:25304800..25307101-chr10:25308254..25310100,3	K562	blood:
12	chr10:25290895..25292994-chr10:25295667..25297503,2	K562	blood:
13	chr10:25305096..25306307-chr16:31190993..31192045,3	Hela-S3	cervix:
14	chr10:25010539..25015061-chr10:25304353..25309032,5	K562	blood:
15	chr10:25009784..25012218-chr10:25304353..25306747,3	K562	blood:
16	chr10:25305870..25307859-chr10:25312050..25313670,2	K562	blood:
17	chr10:24878368..24880293-chr10:25305161..25308124,2	K562	blood:
18	chr10:25010793..25013391-chr10:25309211..25311072,2	MCF-7	breast:
19	chr10:24974642..24976201-chr10:25305799..25307344,2	MCF-7	breast:
20	chr10:24926297..24929907-chr10:25304441..25307349,3	MCF-7	breast:
21	chr10:25304238..25308721-chr10:25308828..25316334,14	MCF-7	breast:
22	chr10:25305518..25306022-chr13:28195597..28196324,2	HCT-116	colon:
23	chr10:25239628..25245194-chr10:25304841..25307327,7	K562	blood:
24	chr10:25294669..25297454-chr10:25303766..25306903,4	K562	blood:
25	chr10:25011203..25013801-chr10:25304621..25307891,5	MCF-7	breast:
26	chr10:25287153..25289677-chr10:25305591..25307248,2	K562	blood:
27	chr10:25295989..25298315-chr10:25301513..25303764,2	K562	blood:
28	chr10:24911061..24913543-chr10:25305498..25307037,2	MCF-7	breast:
29	chr10:25239937..25242303-chr10:25306318..25308090,2	MCF-7	breast:
30	chr10:25295102..25297454-chr10:25303766..25306352,3	K562	blood:
31	chr10:25306123..25307821-chr10:25350955..25353147,2	MCF-7	breast:
32	chr10:25018793..25020691-chr10:25305744..25307257,2	K562	blood:
33	chr10:25295989..25298315-chr10:25301513..25303764,2	K562	blood:
34	chr10:25302483..25304169-chr10:25307134..25309696,2	MCF-7	breast:
35	chr10:25305311..25305983-chr17:7387065..7387884,2	HCT-116	colon:
36	chr10:25302483..25304169-chr10:25307134..25309696,2	MCF-7	breast:
37	chr10:25305234..25306057-chr15:91498102..91498607,2	Hela-S3	cervix:

Variant related genes	Relation type
THNSL1	TF binding region
ENKUR	TF binding region
THNSL1	CpG island
ENKUR	CpG island
ENSG00000273107	chromatin interactions
ENSG00000151023	chromatin interactions
ENSG00000174282	chromatin interactions
ENSG00000181222	chromatin interactions
ENSG00000239039	chromatin interactions
ENSG00000185875	chromatin interactions
ENSG00000186184	chromatin interactions
ENSG00000258384	chromatin interactions
ENSG00000166965	chromatin interactions
ENSG00000089280	chromatin interactions
ENSG00000199535	chromatin interactions
ENSG00000107863	chromatin interactions
ENSG00000099256	chromatin interactions
ENSG00000129696	chromatin interactions
ENSG00000075624	chromatin interactions

Extended variants
information (count: 595 )
Associated
traits (count: 41 )

Variant overlapped rSNPs/rCNVs (count:595 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542756903	chr10:25296057-25296058	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs145916728	chr10:25296073-25296074	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs113844360	chr10:25296075-25296076	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs138409540	chr10:25296086-25296087	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs375827130	chr10:25296147-25296148	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs372542841	chr10:25296152-25296153	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs184136548	chr10:25296170-25296171	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs189459730	chr10:25296186-25296187	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs369066833	chr10:25296195-25296196	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs181981587	chr10:25296197-25296198	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs544463460	chr10:25296232-25296233	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs563439876	chr10:25296255-25296256	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs537290968	chr10:25296296-25296297	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs569880425	chr10:25296324-25296325	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs201070755	chr10:25296345-25296346	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs532483229	chr10:25296354-25296355	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs543112774	chr10:25296359-25296360	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs529663941	chr10:25296375-25296376	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs10764517	chr10:25296379-25296380	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs566545756	chr10:25296395-25296396	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs184963298	chr10:25296414-25296415	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs552396867	chr10:25296425-25296426	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs11014344	chr10:25296433-25296434	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs538145213	chr10:25296462-25296463	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs371575499	chr10:25296512-25296513	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs567570306	chr10:25296531-25296532	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs189590832	chr10:25296566-25296567	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs147997761	chr10:25296568-25296569	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs181537004	chr10:25296584-25296585	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs113265117	chr10:25296585-25296586	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs113593878	chr10:25296590-25296591	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs186284792	chr10:25296655-25296656	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs544526892	chr10:25296685-25296686	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs561593118	chr10:25296700-25296701	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs190215296	chr10:25296735-25296736	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs552076979	chr10:25296766-25296767	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs540203636	chr10:25296834-25296835	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs568308252	chr10:25296890-25296891	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs560036997	chr10:25297005-25297006	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs139468795	chr10:25297073-25297074	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs552260675	chr10:25297098-25297099	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs562673408	chr10:25297101-25297102	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs537271713	chr10:25297123-25297124	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs181411042	chr10:25297144-25297145	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs144510281	chr10:25297181-25297182	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs557613627	chr10:25297208-25297209	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs544581711	chr10:25297213-25297214	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs185771049	chr10:25297225-25297226	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs546965150	chr10:25297227-25297228	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs191122205	chr10:25297237-25297238	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:41)

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
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	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
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25295200-25300800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr10:25300200-25304800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr10:25300800-25301400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr10:25301200-25301400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
5	chr10:25301400-25301600	Enhancers	Brain Anterior Caudate	brain
6	chr10:25301400-25303000	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr10:25301400-25303000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr10:25301600-25304200	Weak transcription	A549	lung
9	chr10:25301800-25303200	Weak transcription	Brain Anterior Caudate	brain
10	chr10:25302400-25304800	Weak transcription	Esophagus	oesophagus
11	chr10:25303000-25303400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
12	chr10:25303000-25303600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr10:25303000-25306400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr10:25303200-25304400	Active TSS	Fetal Brain Female	brain
15	chr10:25303200-25306600	Active TSS	Brain Anterior Caudate	brain
16	chr10:25303400-25305600	Active TSS	Cortex derived primary cultured neurospheres	brain
17	chr10:25303600-25303800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr10:25303600-25303800	Enhancers	Brain Angular Gyrus	brain
19	chr10:25303600-25304000	Enhancers	Hela-S3	cervix
20	chr10:25303600-25304200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr10:25303600-25304200	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr10:25303800-25304000	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr10:25303800-25304000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr10:25303800-25304200	Flanking Active TSS	Brain Angular Gyrus	brain
25	chr10:25303800-25304400	Enhancers	Dnd41	blood
26	chr10:25303800-25304600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr10:25303800-25304600	Enhancers	Liver	Liver
28	chr10:25303800-25306200	Active TSS	Brain Germinal Matrix	brain
29	chr10:25303800-25306400	Active TSS	Brain Hippocampus Middle	brain
30	chr10:25303800-25306600	Active TSS	Brain Cingulate Gyrus	brain
31	chr10:25303800-25306600	Active TSS	Brain Inferior Temporal Lobe	brain
32	chr10:25304000-25304400	Weak transcription	Hela-S3	cervix
33	chr10:25304000-25304600	Enhancers	HepG2	liver
34	chr10:25304000-25307000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
35	chr10:25304200-25304400	Enhancers	Brain Angular Gyrus	brain
36	chr10:25304200-25304400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr10:25304200-25304400	Enhancers	A549	lung
38	chr10:25304200-25304400	Enhancers	HMEC	breast
39	chr10:25304200-25304600	Enhancers	NHDF-Ad	bronchial
40	chr10:25304200-25306400	Active TSS	Fetal Brain Male	brain
41	chr10:25304200-25306600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr10:25304400-25304600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr10:25304400-25304600	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr10:25304400-25304600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr10:25304400-25304600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr10:25304400-25304600	Enhancers	Primary B cells from cord blood	blood
47	chr10:25304400-25304600	Enhancers	Primary T cells from cord blood	blood
48	chr10:25304400-25304600	Enhancers	Primary hematopoietic stem cells	blood
49	chr10:25304400-25304600	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr10:25304400-25304600	Enhancers	Primary T helper cells fromperipheralblood	blood

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