Variant report

Variant	esv3411789
Chromosome Location	chr15:52052789-52087519
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:863)
CpG islands
(count:122)
Chromatin interactive
region (count:61)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:863 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:52069207-52069595	K562	blood:	n/a	n/a
2	BATF	chr15:52068424-52068620	GM12878	blood:	n/a	n/a
3	BCLAF1	chr15:52069149-52069580	GM12878	blood:	n/a	n/a
4	BHLHE40	chr15:52068325-52068723	K562	blood:	n/a	n/a
5	BRCA1	chr15:52068505-52068705	HepG2	liver:	n/a	n/a
6	CBX3	chr15:52074501-52075007	HCT-116	colon:	n/a	n/a
7	CBX3	chr15:52074527-52075001	K562	blood:	n/a	n/a
8	CBX3	chr15:52074597-52074893	K562	blood:	n/a	n/a
9	CEBPB	chr15:52069163-52069552	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr15:52069136-52069564	K562	blood:	n/a	n/a
11	CEBPB	chr15:52072855-52073240	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr15:52053227-52053687	MCF-7	breast:	n/a	chr15:52053454-52053465 chr15:52053453-52053466 chr15:52053455-52053464 chr15:52053453-52053464 chr15:52053453-52053466
13	CEBPB	chr15:52069164-52069540	K562	blood:	n/a	n/a
14	CEBPB	chr15:52069264-52069449	HepG2	liver:	n/a	n/a
15	CEBPB	chr15:52068950-52069666	MCF-7	breast:	n/a	n/a
16	CEBPB	chr15:52069118-52069534	A549	lung:	n/a	n/a
17	CEBPB	chr15:52069025-52069588	MCF-7	breast:	n/a	n/a
18	CEBPB	chr15:52072868-52073279	MCF-7	breast:	n/a	n/a
19	CEBPB	chr15:52053110-52053599	MCF-7	breast:	n/a	chr15:52053454-52053465 chr15:52053453-52053466 chr15:52053455-52053464 chr15:52053453-52053464 chr15:52053453-52053466
20	CEBPB	chr15:52053304-52053579	IMR90	lung:	n/a	chr15:52053454-52053465 chr15:52053453-52053466 chr15:52053455-52053464 chr15:52053453-52053464 chr15:52053453-52053466
21	CEBPB	chr15:52072821-52073312	MCF-7	breast:	n/a	n/a
22	CEBPB	chr15:52069210-52069520	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr15:52072910-52073137	HepG2	liver:	n/a	n/a
24	CEBPB	chr15:52053297-52053643	HepG2	liver:	n/a	chr15:52053454-52053465 chr15:52053453-52053466 chr15:52053455-52053464 chr15:52053453-52053464 chr15:52053453-52053466
25	CEBPB	chr15:52069050-52069611	A549	lung:	n/a	n/a
26	CEBPB	chr15:52069130-52069505	IMR90	lung:	n/a	n/a
27	CEBPB	chr15:52053297-52053603	Hela-S3	cervix:	n/a	chr15:52053454-52053465 chr15:52053453-52053466 chr15:52053455-52053464 chr15:52053453-52053464 chr15:52053453-52053466
28	CEBPB	chr15:52069080-52069512	HepG2	liver:	n/a	n/a
29	CEBPB	chr15:52072962-52073187	A549	lung:	n/a	n/a
30	CHD1	chr15:52068291-52068899	IMR90	lung:	n/a	n/a
31	CHD2	chr15:52079398-52079552	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr15:52079387-52079602	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr15:52068450-52068674	SK-N-SH_RA	brain:	n/a	chr15:52068558-52068576 chr15:52068560-52068573 chr15:52068561-52068571
34	CTCF	chr15:52069340-52069490	NB4	blood:	n/a	chr15:52069377-52069393 chr15:52069371-52069392 chr15:52069378-52069391 chr15:52069376-52069394
35	CTCF	chr15:52074640-52074790	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr15:52068520-52068670	GM12873	blood:	n/a	chr15:52068558-52068576 chr15:52068560-52068573 chr15:52068561-52068571
37	CTCF	chr15:52069280-52069430	AG09309	skin:	n/a	chr15:52069377-52069393 chr15:52069371-52069392 chr15:52069378-52069391 chr15:52069376-52069394
38	CTCF	chr15:52068520-52068670	GM12868	blood:	n/a	chr15:52068558-52068576 chr15:52068560-52068573 chr15:52068561-52068571
39	CTCF	chr15:52074706-52074779	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr15:52074600-52074750	GM12874	blood:	n/a	n/a
41	CTCF	chr15:52069660-52069810	AG04449	skin:	n/a	n/a
42	CTCF	chr15:52079528-52079686	MCF-7	breast:	n/a	n/a
43	CTCF	chr15:52079440-52079590	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr15:52069251-52069497	Kidney_OC	kidney:	n/a	chr15:52069377-52069393 chr15:52069371-52069392 chr15:52069378-52069391 chr15:52069376-52069394
45	CTCF	chr15:52069566-52069571	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr15:52068480-52068630	HCT-116	colon:	n/a	chr15:52068558-52068576 chr15:52068560-52068573 chr15:52068561-52068571
47	CTCF	chr15:52068500-52068650	HPAF	blood vessel:	n/a	chr15:52068558-52068576 chr15:52068560-52068573 chr15:52068561-52068571
48	CTCF	chr15:52079854-52079965	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr15:52069280-52069430	K562	blood:	n/a	chr15:52069377-52069393 chr15:52069371-52069392 chr15:52069378-52069391 chr15:52069376-52069394
50	CTCF	chr15:52068500-52068650	GM12869	blood:	n/a	chr15:52068558-52068576 chr15:52068560-52068573 chr15:52068561-52068571

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:52069389-52069439	BJ	skin:	n/a
2	chr15:52069389-52069439	HPAEpiC	pulmonary alveolar:	n/a
3	chr15:52058531-52058581	H1-hESC	embryonic stem cell:	embryo
4	chr15:52058531-52058581	HCPEpiC	choroid plexus:	n/a
5	chr15:52058531-52058581	K562	blood:	n/a
6	chr15:52058531-52058581	Hepatocyte	liver:	n/a
7	chr15:52069389-52069439	MCF10A-Er-Src	breast:	n/a
8	chr15:52058531-52058581	AG09319	gingival:	n/a
9	chr15:52058531-52058581	AoSMC	blood vessel:	n/a
10	chr15:52069389-52069439	HEK293	kidney:	embryo
11	chr15:52069389-52069439	HNPCEpiC	eye:	n/a
12	chr15:52069389-52069439	Caco-2	colon:	n/a
13	chr15:52058531-52058581	HCT-116	colon:	n/a
14	chr15:52058531-52058581	HNPCEpiC	eye:	n/a
15	chr15:52058531-52058581	AG04450	lung:	fetal
16	chr15:52069389-52069439	HRCEpiC	kidney:	n/a
17	chr15:52058531-52058581	SK-N-MC	brain:	n/a
18	chr15:52058531-52058581	PFSK-1	brain:	n/a
19	chr15:52069389-52069439	HMEC	breast:	n/a
20	chr15:52058531-52058581	HMEC	breast:	n/a
21	chr15:52058531-52058581	SK-N-SH	brain:	n/a
22	chr15:52058531-52058581	CMK	blood:	n/a
23	chr15:52058531-52058581	HCM	heart:	n/a
24	chr15:52069389-52069439	HRPEpiC	eye:	n/a
25	chr15:52058531-52058581	SAEC	small airway:	n/a
26	chr15:52069389-52069439	NHBE	bronchial:	n/a
27	chr15:52058531-52058581	HRPEpiC	eye:	n/a
28	chr15:52058531-52058581	HIPEpiC	eye:	n/a
29	chr15:52058531-52058581	NB4	blood:	n/a
30	chr15:52058531-52058581	HEK293	kidney:	embryo
31	chr15:52058531-52058581	HCF	heart:	n/a
32	chr15:52069389-52069439	PrEC	prostate:	n/a
33	chr15:52069389-52069439	HAEpiC	amniotic membrane:	n/a
34	chr15:52058531-52058581	RPTEC	kidney:	n/a
35	chr15:52069389-52069439	HL-60	blood:	n/a
36	chr15:52069389-52069439	GM12891	blood:	n/a
37	chr15:52058531-52058581	GM12878	blood:	n/a
38	chr15:52069389-52069439	HUVEC	blood vessel:	n/a
39	chr15:52069389-52069439	HIPEpiC	eye:	n/a
40	chr15:52069389-52069439	HCT-116	colon:	n/a
41	chr15:52058531-52058581	HAEpiC	amniotic membrane:	n/a
42	chr15:52058531-52058581	U87	brain:	n/a
43	chr15:52058531-52058581	ECC-1	luminal epithelium:	n/a
44	chr15:52069389-52069439	GM19239	blood:	n/a
45	chr15:52069389-52069439	H1-hESC	embryonic stem cell:	embryo
46	chr15:52058531-52058581	ProgFib	skin:	n/a
47	chr15:52058531-52058581	SK-N-SH_RA	brain:	n/a
48	chr15:52069389-52069439	BE2_C	brain:	n/a
49	chr15:52069389-52069439	Jurkat	blood:	n/a
50	chr15:52069389-52069439	A549	lung:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:163429652..163430349-chr15:52086238..52087036,2	MCF-7	breast:
2	chr15:52046348..52048954-chr15:52084849..52087226,2	K562	blood:
3	chr15:51934747..51936336-chr15:52066593..52068125,2	MCF-7	breast:
4	chr15:51941554..51943046-chr15:52068074..52069805,23	MCF-7	breast:
5	chr15:52035146..52037140-chr15:52056300..52058053,2	MCF-7	breast:
6	chr15:52068475..52069079-chr5:175843322..175844018,2	MCF-7	breast:
7	chr15:51942270..51945778-chr15:52064444..52070724,6	MCF-7	breast:
8	chr15:52054450..52058295-chr15:52061213..52063877,3	MCF-7	breast:
9	chr15:52041772..52043796-chr15:52059873..52062736,2	MCF-7	breast:
10	chr15:51960322..51962005-chr15:52066189..52068560,2	MCF-7	breast:
11	chr15:52058591..52061806-chr15:52062033..52065705,3	K562	blood:
12	chr15:51914398..51916260-chr15:52068370..52070743,2	MCF-7	breast:
13	chr15:52072025..52074741-chr15:52120265..52123225,4	MCF-7	breast:
14	chr15:52068385..52068980-chr15:52199769..52200319,2	MCF-7	breast:
15	chr15:52086963..52088898-chr15:52262138..52264722,2	MCF-7	breast:
16	chr15:51944344..51944987-chr15:52068324..52069242,2	K562	blood:
17	chr15:52071058..52073972-chr15:52076108..52078504,2	MCF-7	breast:
18	chr15:52072134..52075031-chr15:52213597..52215274,2	MCF-7	breast:
19	chr15:52028103..52031226-chr15:52067709..52070826,4	MCF-7	breast:
20	chr15:51915397..51918003-chr15:52069309..52070981,2	MCF-7	breast:
21	chr15:52049654..52051374-chr15:52054509..52056705,2	MCF-7	breast:
22	chr15:52071204..52073372-chr15:52073391..52075990,2	MCF-7	breast:
23	chr15:52066782..52068906-chr15:52166173..52168247,2	K562	blood:
24	chr15:52043955..52045654-chr15:52058986..52062034,3	MCF-7	breast:
25	chr15:51941765..51942808-chr15:52067729..52069864,21	K562	blood:
26	chr15:52063986..52066845-chr15:52067763..52069392,2	MCF-7	breast:
27	chr15:51939054..51940894-chr15:52070011..52072606,2	MCF-7	breast:
28	chr15:52054450..52058295-chr15:52061213..52063877,3	MCF-7	breast:
29	chr15:52077466..52080327-chr15:52092211..52093843,2	MCF-7	breast:
30	chr15:51938680..51944458-chr15:52065543..52071230,9	K562	blood:
31	chr15:52049744..52051270-chr15:52058518..52061301,2	K562	blood:
32	chr15:52062590..52065272-chr15:52121050..52123108,2	MCF-7	breast:
33	chr15:52073675..52076293-chr15:52262420..52265302,2	MCF-7	breast:
34	chr15:52068908..52069729-chr15:52209041..52209994,3	MCF-7	breast:
35	chr15:52047517..52051526-chr15:52055116..52057120,3	K562	blood:
36	chr15:52026672..52029372-chr15:52056834..52058990,2	MCF-7	breast:
37	chr15:51939928..51943794-chr15:52067782..52071460,6	MCF-7	breast:
38	chr15:52074262..52074783-chr15:52431783..52432627,2	MCF-7	breast:
39	chr15:51970684..51971589-chr15:52068849..52069771,2	MCF-7	breast:
40	chr15:52068524..52069693-chr15:52209370..52210387,3	MCF-7	breast:
41	chr15:52044048..52045789-chr15:52054903..52057784,2	MCF-7	breast:
42	chr15:52071204..52073372-chr15:52073391..52075990,2	MCF-7	breast:
43	chr15:52041578..52043683-chr15:52065420..52068365,2	K562	blood:
44	chr15:52063986..52066845-chr15:52067763..52069392,2	MCF-7	breast:
45	chr15:51942308..51943114-chr15:52068750..52069400,2	MCF-7	breast:
46	chr15:52028181..52032954-chr15:52050508..52053619,6	MCF-7	breast:
47	chr15:52074623..52075189-chr15:52431810..52432342,2	K562	blood:
48	chr15:52071321..52074509-chr15:52077480..52080021,3	MCF-7	breast:
49	chr15:52058591..52061806-chr15:52062033..52065705,3	K562	blood:
50	chr15:51941637..51943668-chr15:52068078..52069917,57	MCF-7	breast:

No data

Variant related genes	Relation type
TMOD2	TF binding region
TMOD2	CpG island
ENSG00000259377	chromatin interactions
ENSG00000175416	chromatin interactions
ENSG00000140280	chromatin interactions
ENSG00000128872	chromatin interactions
ENSG00000138594	chromatin interactions
ENSG00000166477	chromatin interactions
ENSG00000069966	chromatin interactions
ENSG00000272337	chromatin interactions
ENSG00000104093	chromatin interactions

Extended variants
information (count: 1316 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1316 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2652597	chr15:52052818-52052819	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs138065054	chr15:52052825-52052826	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs149536961	chr15:52052867-52052868	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs539879214	chr15:52052886-52052887	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs145947817	chr15:52052928-52052929	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs574944328	chr15:52052943-52052944	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs186528649	chr15:52052958-52052959	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs8032945	chr15:52053010-52053011	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs11459575	chr15:52053011-52053012	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs397686415	chr15:52053020-52053021	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs563699610	chr15:52053023-52053024	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs138869024	chr15:52053054-52053055	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs555286894	chr15:52053100-52053101	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs539921353	chr15:52053137-52053138	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs1545602	chr15:52053156-52053157	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs17649047	chr15:52053229-52053230	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs191386264	chr15:52053245-52053246	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs181578435	chr15:52053246-52053247	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs117812931	chr15:52053277-52053278	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs185686219	chr15:52053336-52053337	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs373493635	chr15:52053350-52053351	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs542674781	chr15:52053375-52053376	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs142740227	chr15:52053390-52053391	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs200322767	chr15:52053424-52053425	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs5812567	chr15:52053454-52053455	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs533451873	chr15:52053457-52053458	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs570360034	chr15:52053488-52053489	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs563534105	chr15:52053499-52053500	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs4603504	chr15:52053500-52053501	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs368315582	chr15:52053540-52053541	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs529534674	chr15:52053544-52053545	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs376968775	chr15:52053569-52053570	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs563207367	chr15:52053592-52053593	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs73407332	chr15:52053638-52053639	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs113191147	chr15:52053643-52053644	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs190986296	chr15:52053652-52053653	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs537583646	chr15:52053660-52053661	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs368968317	chr15:52053737-52053738	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs11446560	chr15:52053767-52053768	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs527791909	chr15:52053776-52053777	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs183128037	chr15:52053794-52053795	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs567652361	chr15:52053823-52053824	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs560598393	chr15:52053871-52053872	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs535147323	chr15:52053893-52053894	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs74717096	chr15:52053935-52053936	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs538085295	chr15:52053937-52053938	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs372271513	chr15:52053976-52053977	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs547324506	chr15:52054067-52054068	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs553176911	chr15:52054073-52054074	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs571236703	chr15:52054097-52054098	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:841 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:52044600-52060000	Weak transcription	Esophagus	oesophagus
2	chr15:52044600-52060200	Weak transcription	Aorta	Aorta
3	chr15:52044800-52060000	Weak transcription	Spleen	Spleen
4	chr15:52045000-52060200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr15:52045200-52053400	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr15:52045800-52053200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
7	chr15:52046800-52060000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr15:52047200-52053600	Enhancers	Brain Cingulate Gyrus	brain
9	chr15:52047400-52053600	Enhancers	Brain Hippocampus Middle	brain
10	chr15:52048000-52058000	Weak transcription	Primary T cells from cord blood	blood
11	chr15:52048200-52060000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr15:52048200-52060200	Weak transcription	Thymus	Thymus
13	chr15:52049000-52053000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr15:52049200-52053000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr15:52049200-52053400	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr15:52049200-52060000	Weak transcription	Dnd41	blood
17	chr15:52049400-52059800	Weak transcription	Primary B cells from cord blood	blood
18	chr15:52049800-52053400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr15:52049800-52059800	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr15:52051200-52060000	Weak transcription	Fetal Muscle Trunk	muscle
21	chr15:52051200-52060000	Weak transcription	Lung	lung
22	chr15:52051200-52077600	Weak transcription	Psoas Muscle	Psoas
23	chr15:52051400-52053400	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr15:52051400-52053600	Enhancers	Brain Substantia Nigra	brain
25	chr15:52051400-52060000	Weak transcription	Fetal Brain Female	brain
26	chr15:52051400-52060200	Weak transcription	Adipose Nuclei	Adipose
27	chr15:52051400-52060400	Weak transcription	Stomach Smooth Muscle	stomach
28	chr15:52051400-52061200	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr15:52051400-52068400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr15:52051400-52068400	Weak transcription	Stomach Mucosa	stomach
31	chr15:52052200-52056800	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr15:52052200-52060000	Weak transcription	Left Ventricle	heart
33	chr15:52052200-52060000	Weak transcription	Ovary	ovary
34	chr15:52052200-52060200	Weak transcription	Right Ventricle	heart
35	chr15:52052200-52060800	Weak transcription	Colon Smooth Muscle	Colon
36	chr15:52052200-52061200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr15:52052200-52064200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr15:52052200-52068200	Weak transcription	Fetal Intestine Small	intestine
39	chr15:52052200-52068600	Weak transcription	HMEC	breast
40	chr15:52052200-52074600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr15:52052200-52076000	Weak transcription	Fetal Brain Male	brain
42	chr15:52052200-52101800	Weak transcription	Colonic Mucosa	Colon
43	chr15:52052400-52052800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr15:52052400-52053600	Weak transcription	Right Atrium	heart
45	chr15:52052400-52060000	Weak transcription	Fetal Muscle Leg	muscle
46	chr15:52052400-52060200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr15:52052400-52060200	Weak transcription	Fetal Lung	lung
48	chr15:52052400-52060600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr15:52052400-52061000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr15:52052400-52067000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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