Variant report

Variant	esv3365935
Chromosome Location	chrX:139012861-139016459
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:751)
CpG islands
(count:429)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:751 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:139013394-139013604	HepG2	liver:	n/a	n/a
2	ARID3A	chrX:139012775-139013271	K562	blood:	n/a	n/a
3	ARID3A	chrX:139015623-139015830	K562	blood:	n/a	n/a
4	BACH1	chrX:139014004-139014182	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chrX:139013237-139013318	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chrX:139015363-139015476	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chrX:139012613-139012895	GM12878	blood:	n/a	n/a
8	BCLAF1	chrX:139014871-139015227	GM12878	blood:	n/a	n/a
9	BHLHE40	chrX:139013392-139013522	GM12878	blood:	n/a	n/a
10	BHLHE40	chrX:139013983-139015969	K562	blood:	n/a	chrX:139014481-139014497
11	BHLHE40	chrX:139014022-139014564	GM12878	blood:	n/a	chrX:139014481-139014497
12	BHLHE40	chrX:139013415-139013752	K562	blood:	n/a	n/a
13	BHLHE40	chrX:139015014-139015440	GM12878	blood:	n/a	n/a
14	BRCA1	chrX:139015405-139015599	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chrX:139015279-139015665	Hela-S3	cervix:	n/a	n/a
16	CBX3	chrX:139015022-139015577	K562	blood:	n/a	n/a
17	CCNT2	chrX:139014128-139015086	K562	blood:	n/a	chrX:139015008-139015017 chrX:139014461-139014481
18	CEBPB	chrX:139015428-139015628	H1-hESC	embryonic stem cell:	n/a	chrX:139015512-139015523 chrX:139015512-139015523
19	CEBPB	chrX:139015085-139015933	Hela-S3	cervix:	n/a	chrX:139015512-139015523 chrX:139015512-139015523
20	CEBPB	chrX:139015041-139015161	K562	blood:	n/a	n/a
21	CEBPD	chrX:139014370-139014765	K562	blood:	n/a	n/a
22	CEBPD	chrX:139015241-139015386	HepG2	liver:	n/a	n/a
23	CEBPD	chrX:139014109-139014719	K562	blood:	n/a	n/a
24	CHD1	chrX:139014543-139014780	GM12878	blood:	n/a	n/a
25	CHD1	chrX:139015452-139015834	H1-hESC	embryonic stem cell:	n/a	chrX:139015813-139015823
26	CHD1	chrX:139014155-139014243	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chrX:139015027-139015196	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD1	chrX:139013227-139013379	GM12878	blood:	n/a	n/a
29	CHD1	chrX:139012827-139012949	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chrX:139015063-139015205	GM12878	blood:	n/a	n/a
31	CHD1	chrX:139012232-139012913	GM12878	blood:	n/a	n/a
32	CHD2	chrX:139014000-139014156	K562	blood:	n/a	n/a
33	CHD2	chrX:139014804-139015517	K562	blood:	n/a	chrX:139015014-139015024 chrX:139015275-139015285 chrX:139015251-139015261 chrX:139015009-139015019
34	CHD2	chrX:139013494-139013707	GM12878	blood:	n/a	n/a
35	CHD2	chrX:139013478-139013668	K562	blood:	n/a	n/a
36	CHD2	chrX:139015132-139015492	HepG2	liver:	n/a	chrX:139015275-139015285 chrX:139015251-139015261
37	CHD2	chrX:139015003-139015548	GM12878	blood:	n/a	chrX:139015014-139015024 chrX:139015275-139015285 chrX:139015251-139015261 chrX:139015009-139015019
38	CHD2	chrX:139014083-139014254	GM12878	blood:	n/a	n/a
39	CHD2	chrX:139014762-139015918	Hela-S3	cervix:	n/a	chrX:139015014-139015024 chrX:139015275-139015285 chrX:139015251-139015261 chrX:139015813-139015823 chrX:139015009-139015019
40	CHD2	chrX:139014177-139014546	Hela-S3	cervix:	n/a	n/a
41	CHD2	chrX:139015155-139015465	H1-hESC	embryonic stem cell:	n/a	chrX:139015275-139015285 chrX:139015251-139015261
42	CREB1	chrX:139014903-139015538	GM12878	blood:	n/a	n/a
43	CREB1	chrX:139015656-139015908	A549	lung:	n/a	n/a
44	CREB1	chrX:139015005-139015576	A549	lung:	n/a	n/a
45	CTCF	chrX:139015336-139015438	Lung_OC	lung:	n/a	n/a
46	CTCF	chrX:139013220-139013370	HAc	cerebellar:	n/a	n/a
47	CTCF	chrX:139015220-139015370	GM12868	blood:	n/a	n/a
48	CTCF	chrX:139015280-139015430	GM12873	blood:	n/a	n/a
49	CTCF	chrX:139014880-139015030	HPF	lung:	n/a	n/a
50	CTCF	chrX:139014913-139014991	MCF-7	breast:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:139013957-139014007	Hela-S3	cervix:	n/a
2	chrX:139015886-139015936	PFSK-1	brain:	n/a
3	chrX:139013957-139014007	Hela-S3	cervix:	n/a
4	chrX:139015886-139015936	PFSK-1	brain:	n/a
5	chrX:139015490-139015540	PFSK-1	brain:	n/a
6	chrX:139015804-139015854	AoSMC	blood vessel:	n/a
7	chrX:139015886-139015936	HIPEpiC	eye:	n/a
8	chrX:139015886-139015936	NHDF-neo	bronchial:	n/a
9	chrX:139015804-139015854	SK-N-MC	brain:	n/a
10	chrX:139015212-139015262	SK-N-MC	brain:	n/a
11	chrX:139014460-139014510	RPTEC	kidney:	n/a
12	chrX:139014368-139014418	Hela-S3	cervix:	n/a
13	chrX:139015490-139015540	SK-N-MC	brain:	n/a
14	chrX:139015490-139015540	HIPEpiC	eye:	n/a
15	chrX:139015490-139015540	NHBE	bronchial:	n/a
16	chrX:139014460-139014510	K562	blood:	n/a
17	chrX:139015886-139015936	GM06990	blood:	n/a
18	chrX:139013957-139014007	AG10803	skin:	n/a
19	chrX:139014368-139014418	MCF10A-Er-Src	breast:	n/a
20	chrX:139015490-139015540	HRPEpiC	eye:	n/a
21	chrX:139013957-139014007	T-47D	breast:	n/a
22	chrX:139015490-139015540	HAEpiC	amniotic membrane:	n/a
23	chrX:139015212-139015262	HL-60	blood:	n/a
24	chrX:139015804-139015854	SKMC	muscle:	n/a
25	chrX:139015886-139015936	HCPEpiC	choroid plexus:	n/a
26	chrX:139013957-139014007	GM12878	blood:	n/a
27	chrX:139014460-139014510	AG10803	skin:	n/a
28	chrX:139015490-139015540	HPAEpiC	pulmonary alveolar:	n/a
29	chrX:139013957-139014007	HRPEpiC	eye:	n/a
30	chrX:139015212-139015262	NH-A	brain:	n/a
31	chrX:139014368-139014418	RPTEC	kidney:	n/a
32	chrX:139015886-139015936	NH-A	brain:	n/a
33	chrX:139014368-139014418	BJ	skin:	n/a
34	chrX:139015804-139015854	LNCaP	prostate:	n/a
35	chrX:139015886-139015936	HCF	heart:	n/a
36	chrX:139014460-139014510	HL-60	blood:	n/a
37	chrX:139015804-139015854	AG04450	lung:	fetal
38	chrX:139015804-139015854	U87	brain:	n/a
39	chrX:139015804-139015854	BJ	skin:	n/a
40	chrX:139015490-139015540	MCF-7	breast:	n/a
41	chrX:139013957-139014007	NHDF-neo	bronchial:	n/a
42	chrX:139015886-139015936	NT2-D1	testis:	n/a
43	chrX:139015212-139015262	GM12891	blood:	n/a
44	chrX:139014368-139014418	NT2-D1	testis:	n/a
45	chrX:139014368-139014418	BE2_C	brain:	n/a
46	chrX:139013957-139014007	HMEC	breast:	n/a
47	chrX:139014368-139014418	GM12878	blood:	n/a
48	chrX:139014460-139014510	HRE	kidney:	n/a
49	chrX:139015490-139015540	Caco-2	colon:	n/a
50	chrX:139014460-139014510	MCF10A-Er-Src	breast:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:138963273..138965824-chrX:139016270..139017818,2	K562	blood:
2	chr17:4853164..4854128-chrX:139015400..139015911,2	Hela-S3	cervix:
3	chr12:120632818..120635687-chrX:139013169..139015173,2	K562	blood:
4	chrX:138985114..138987559-chrX:139013389..139015006,2	K562	blood:
5	chrX:138956213..138958123-chrX:139012738..139014426,2	MCF-7	breast:
6	chr19:30432737..30433705-chrX:139015015..139015718,2	Hela-S3	cervix:
7	chrX:138988048..138990751-chrX:139013105..139014679,2	K562	blood:
8	chrX:139003030..139006775-chrX:139014135..139016470,3	MCF-7	breast:
9	chrX:139003050..139005893-chrX:139011125..139013950,3	MCF-7	breast:
10	chrX:138906465..138908031-chrX:139012823..139014377,2	MCF-7	breast:
11	chrX:139012765..139014914-chrX:139031974..139034930,2	K562	blood:
12	chrX:139013823..139015726-chrX:139026324..139028127,2	MCF-7	breast:
13	chrX:138953765..138955836-chrX:139011529..139013687,2	K562	blood:
14	chrX:138909179..138912021-chrX:139015740..139017279,2	K562	blood:
15	chr11:122932486..122933259-chrX:139015343..139016082,2	NB4	blood:
16	chrX:138772808..138775259-chrX:139014635..139016368,2	MCF-7	breast:
17	chr16:81737296..81737796-chrX:139014881..139015641,2	NB4	blood:
18	chrX:138931759..138934021-chrX:139013116..139015222,2	MCF-7	breast:
19	chrX:139011779..139014233-chrX:139015121..139017109,2	MCF-7	breast:

No data

Variant related genes	Relation type
ATP11C	TF binding region
ATP11C	CpG island
ENSG00000101977	chromatin interactions
ENSG00000108515	chromatin interactions
ENSG00000153815	chromatin interactions
ENSG00000105176	chromatin interactions
ENSG00000089157	chromatin interactions
ENSG00000109971	chromatin interactions
ENSG00000101974	chromatin interactions
ENSG00000207633	chromatin interactions

Extended variants
information (count: 44 )
Associated
traits (count: 44 )

Variant overlapped rSNPs/rCNVs (count:44 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186787184	chrX:139012976-139012977	Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs556115873	chrX:139013007-139013008	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs190877377	chrX:139013142-139013143	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs183066549	chrX:139013315-139013316	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs113710120	chrX:139013383-139013384	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs72617910	chrX:139013429-139013430	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs189091871	chrX:139013434-139013435	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs555593527	chrX:139013445-139013446	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs145937421	chrX:139013450-139013451	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs35739294	chrX:139013567-139013568	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs370241502	chrX:139013649-139013650	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs4824921	chrX:139013712-139013713	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs34668100	chrX:139013750-139013751	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs375382218	chrX:139013824-139013825	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs113162025	chrX:139013892-139013893	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs34429201	chrX:139013907-139013908	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs368498961	chrX:139013994-139013995	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs34761367	chrX:139013995-139013996	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs35625463	chrX:139013997-139013998	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs34901135	chrX:139014024-139014025	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs371148529	chrX:139014239-139014240	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs372027127	chrX:139014241-139014242	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs374083313	chrX:139014294-139014295	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs192833425	chrX:139014338-139014339	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs367931445	chrX:139014448-139014449	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs371537028	chrX:139014514-139014515	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs111861577	chrX:139014598-139014599	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs374765959	chrX:139014621-139014622	Active TSS ZNF genes & repeats Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs367557158	chrX:139014643-139014644	Active TSS ZNF genes & repeats Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs372370666	chrX:139014808-139014809	Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs201534712	chrX:139015478-139015479	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs56783764	chrX:139015481-139015482	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs185373911	chrX:139015734-139015735	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs376703942	chrX:139015895-139015896	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs187893938	chrX:139015930-139015931	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs539929350	chrX:139016013-139016014	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs191896271	chrX:139016036-139016037	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs12010760	chrX:139016215-139016216	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs183751240	chrX:139016238-139016239	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs188476131	chrX:139016262-139016263	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs529276986	chrX:139016344-139016345	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs4825170	chrX:139016394-139016395	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs368733762	chrX:139016395-139016396	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs373584415	chrX:139016425-139016426	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:44)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Burkitt''s lymphoma	20823134	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Astrocytoma	17387387	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	21979893	CNVD
Schizophrenia	23904455	CNVD
Olfactory neuroblastoma	18408657	CNVD
infertile	22614455	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Cancer	16751803	CNVD
small cell lung cancer	20016488	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	17603634	CNVD
abnormal development	18461090	CNVD
Multiple myeloma	17550852	CNVD
Premature ovarian failure	20952765	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Hereditary coagulopathy	21993689	CNVD
Cerebellar atrophy	21569638	CNVD
Fragile x	21569638	CNVD
Abnormal corpus callosum	21572526	CNVD
Congenital diaphragmatic hernia	21525063	CNVD

Chromatin state (count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:138998600-139013200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chrX:139003000-139013000	Weak transcription	Fetal Heart	heart
3	chrX:139003000-139013200	Weak transcription	Psoas Muscle	Psoas
4	chrX:139005000-139013200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chrX:139006800-139013200	Weak transcription	Primary T cells fromperipheralblood	blood
6	chrX:139006800-139013200	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chrX:139007000-139013200	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chrX:139010400-139013200	Weak transcription	Aorta	Aorta
9	chrX:139011000-139016000	Active TSS	GM12878-XiMat	blood
10	chrX:139011800-139013000	Enhancers	Primary T cells from cord blood	blood
11	chrX:139011800-139016800	Active TSS	HepG2	liver
12	chrX:139012000-139013000	Enhancers	Fetal Brain Male	brain
13	chrX:139012000-139013800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
14	chrX:139012000-139016000	Active TSS	NHEK	skin
15	chrX:139012200-139013000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
16	chrX:139012200-139013000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
17	chrX:139012200-139013000	Flanking Active TSS	Liver	Liver
18	chrX:139012200-139013000	Flanking Active TSS	K562	blood
19	chrX:139012200-139013200	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chrX:139012200-139013200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chrX:139012200-139013200	Enhancers	Primary T killer memory cells from peripheral blood	blood
22	chrX:139012200-139013200	Enhancers	Colon Smooth Muscle	Colon
23	chrX:139012200-139013200	Enhancers	Right Ventricle	heart
24	chrX:139012200-139013200	Flanking Active TSS	HUVEC	blood vessel
25	chrX:139012200-139013600	Flanking Active TSS	Dnd41	blood
26	chrX:139012200-139016000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chrX:139012200-139016200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
28	chrX:139012200-139016200	Active TSS	NHDF-Ad	bronchial
29	chrX:139012200-139016400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chrX:139012200-139016400	Active TSS	NHLF	lung
31	chrX:139012400-139013000	Weak transcription	Fetal Thymus	thymus
32	chrX:139012400-139013200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chrX:139012400-139013200	Bivalent/Poised TSS	Fetal Kidney	kidney
34	chrX:139012400-139013200	Enhancers	HSMMtube	muscle
35	chrX:139012400-139013400	Weak transcription	Gastric	stomach
36	chrX:139012400-139016200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chrX:139012400-139016400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chrX:139012600-139013000	Flanking Active TSS	H9 Cell Line	embryonic stem cell
39	chrX:139012600-139013000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
40	chrX:139012600-139013000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
41	chrX:139012600-139013000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chrX:139012600-139013000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
43	chrX:139012600-139013000	Enhancers	Primary B cells from cord blood	blood
44	chrX:139012600-139013000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
45	chrX:139012600-139013000	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chrX:139012600-139013000	Enhancers	Brain Hippocampus Middle	brain
47	chrX:139012600-139013000	Flanking Active TSS	Fetal Intestine Small	intestine
48	chrX:139012600-139013000	Enhancers	Rectal Smooth Muscle	rectum
49	chrX:139012600-139013000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
50	chrX:139012600-139013000	Flanking Active TSS	HMEC	breast

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