Variant report

Variant	esv3367526
Chromosome Location	chr12:57109835-57113733
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:200)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:200 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr12:57110520-57110670	GM12866	blood:	n/a	n/a
2	EP300	chr12:57111548-57111863	GM12878	blood:	n/a	n/a
3	EP300	chr12:57111556-57111748	GM12878	blood:	n/a	n/a
4	HEY1	chr12:57111571-57111955	HepG2	liver:	n/a	n/a
5	HEY1	chr12:57111470-57111835	K562	blood:	n/a	n/a
6	HEY1	chr12:57109521-57110035	K562	blood:	n/a	n/a
7	HEY1	chr12:57113606-57114096	K562	blood:	n/a	n/a
8	HEY1	chr12:57111540-57111862	HepG2	liver:	n/a	n/a
9	HEY1	chr12:57110055-57110696	K562	blood:	n/a	n/a
10	HEY1	chr12:57112810-57113091	K562	blood:	n/a	n/a
11	HEY1	chr12:57110928-57111323	K562	blood:	n/a	n/a
12	HEY1	chr12:57111440-57112682	K562	blood:	n/a	n/a
13	MTA3	chr12:57112012-57112430	GM12878	blood:	n/a	n/a
14	MTA3	chr12:57109628-57110229	GM12878	blood:	n/a	n/a
15	POLR2A	chr12:57112836-57113480	MCF-7	breast:	n/a	n/a
16	POLR2A	chr12:57112650-57113668	HepG2	liver:	n/a	n/a
17	POLR2A	chr12:57112099-57112225	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr12:57112815-57113251	ECC-1	luminal epithelium:	n/a	n/a
19	POLR2A	chr12:57109223-57113587	K562	blood:	n/a	n/a
20	POLR2A	chr12:57111127-57111323	GM12878	blood:	n/a	n/a
21	POLR2A	chr12:57110383-57110503	A549	lung:	n/a	n/a
22	POLR2A	chr12:57109342-57110329	HepG2	liver:	n/a	n/a
23	POLR2A	chr12:57110914-57111196	GM12891	blood:	n/a	n/a
24	POLR2A	chr12:57109177-57115890	PFSK-1	brain:	n/a	n/a
25	POLR2A	chr12:57110092-57110514	HepG2	liver:	n/a	n/a
26	POLR2A	chr12:57112304-57112316	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr12:57109523-57109965	A549	lung:	n/a	n/a
28	POLR2A	chr12:57109520-57110076	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr12:57112015-57112031	MCF-7	breast:	n/a	n/a
30	POLR2A	chr12:57111783-57111806	MCF-7	breast:	n/a	n/a
31	POLR2A	chr12:57109238-57110415	GM12891	blood:	n/a	n/a
32	POLR2A	chr12:57112892-57113039	SK-N-SH	brain:	n/a	n/a
33	POLR2A	chr12:57111468-57111696	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr12:57109501-57110656	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr12:57111980-57112006	MCF-7	breast:	n/a	n/a
36	POLR2A	chr12:57113204-57113365	MCF10A-Er-Src	breast:	n/a	n/a
37	POLR2A	chr12:57112667-57112678	ProgFib	skin:	n/a	n/a
38	POLR2A	chr12:57111018-57111371	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr12:57109481-57110867	ECC-1	luminal epithelium:	n/a	n/a
40	POLR2A	chr12:57109094-57117058	SK-N-MC	brain:	n/a	n/a
41	POLR2A	chr12:57112826-57113161	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr12:57113250-57113647	K562	blood:	n/a	n/a
43	POLR2A	chr12:57109763-57110607	U87	brain:	n/a	n/a
44	POLR2A	chr12:57110739-57111235	GM12892	blood:	n/a	n/a
45	POLR2A	chr12:57112176-57112495	A549	lung:	n/a	n/a
46	POLR2A	chr12:57112347-57112635	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr12:57113476-57113810	HepG2	liver:	n/a	n/a
48	POLR2A	chr12:57109930-57110637	K562	blood:	n/a	n/a
49	POLR2A	chr12:57111868-57112834	HL-60	blood:	n/a	n/a
50	POLR2A	chr12:57110955-57110956	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:57113463-57113513	MCF-7	breast:	n/a
2	chr12:57113463-57113513	GM12892	blood:	n/a
3	chr12:57113463-57113513	H1-hESC	embryonic stem cell:	embryo
4	chr12:57113463-57113513	HCM	heart:	n/a
5	chr12:57113463-57113513	GM06990	blood:	n/a
6	chr12:57113463-57113513	LNCaP	prostate:	n/a
7	chr12:57113463-57113513	ECC-1	luminal epithelium:	n/a
8	chr12:57113463-57113513	SK-N-SH_RA	brain:	n/a
9	chr12:57113463-57113513	GM12878	blood:	n/a
10	chr12:57113463-57113513	K562	blood:	n/a
11	chr12:57113463-57113513	HCPEpiC	choroid plexus:	n/a
12	chr12:57113463-57113513	HUVEC	blood vessel:	n/a
13	chr12:57113463-57113513	HL-60	blood:	n/a
14	chr12:57113463-57113513	GM12891	blood:	n/a
15	chr12:57113463-57113513	HNPCEpiC	eye:	n/a
16	chr12:57113463-57113513	HCT-116	colon:	n/a
17	chr12:57113463-57113513	AG04450	lung:	fetal
18	chr12:57113463-57113513	IMR90	lung:	fetal
19	chr12:57113463-57113513	AoSMC	blood vessel:	n/a
20	chr12:57113463-57113513	ProgFib	skin:	n/a
21	chr12:57113463-57113513	HepG2	liver:	n/a
22	chr12:57113463-57113513	Hepatocyte	liver:	n/a
23	chr12:57113463-57113513	AG09319	gingival:	n/a
24	chr12:57113463-57113513	AG10803	skin:	n/a
25	chr12:57113463-57113513	SAEC	small airway:	n/a
26	chr12:57113463-57113513	T-47D	breast:	n/a
27	chr12:57113463-57113513	HMEC	breast:	n/a
28	chr12:57113463-57113513	HCF	heart:	n/a
29	chr12:57113463-57113513	MCF10A-Er-Src	breast:	n/a
30	chr12:57113463-57113513	NH-A	brain:	n/a
31	chr12:57113463-57113513	HAEpiC	amniotic membrane:	n/a
32	chr12:57113463-57113513	NHDF-neo	bronchial:	n/a
33	chr12:57113463-57113513	HEK293	kidney:	embryo
34	chr12:57113463-57113513	AG09309	skin:	n/a
35	chr12:57113463-57113513	PrEC	prostate:	n/a
36	chr12:57113463-57113513	Caco-2	colon:	n/a
37	chr12:57113463-57113513	BE2_C	brain:	n/a
38	chr12:57113463-57113513	CMK	blood:	n/a
39	chr12:57113463-57113513	SK-N-SH	brain:	n/a
40	chr12:57113463-57113513	U87	brain:	n/a
41	chr12:57113463-57113513	A549	lung:	n/a
42	chr12:57113463-57113513	RPTEC	kidney:	n/a
43	chr12:57113463-57113513	GM19239	blood:	n/a
44	chr12:57113463-57113513	HPAEpiC	pulmonary alveolar:	n/a
45	chr12:57113463-57113513	PFSK-1	brain:	n/a
46	chr12:57113463-57113513	Jurkat	blood:	n/a
47	chr12:57113463-57113513	SK-N-MC	brain:	n/a
48	chr12:57113463-57113513	HRPEpiC	eye:	n/a
49	chr12:57113463-57113513	HEEpiC	esophagus:	n/a
50	chr12:57113463-57113513	HIPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:57076604..57085974-chr12:57112559..57120474,46	MCF-7	breast:
2	chr12:57038025..57041646-chr12:57113711..57120620,12	MCF-7	breast:
3	chr12:57113156..57115169-chr12:57146013..57147663,2	K562	blood:
4	chr12:57022951..57032187-chr12:57113330..57121462,17	K562	blood:
5	chr12:57025967..57028369-chr12:57109076..57111615,2	K562	blood:
6	chr12:57029529..57031708-chr12:57108822..57111712,2	K562	blood:
7	chr12:57074578..57085543-chr12:57108746..57121559,55	K562	blood:
8	chr12:57078008..57083064-chr12:57107591..57112002,6	MCF-7	breast:
9	chr12:57091435..57092961-chr12:57113686..57115355,2	K562	blood:
10	chr12:56510526..56513327-chr12:57111291..57113363,2	K562	blood:
11	chr12:57098172..57100413-chr12:57108972..57110548,2	MCF-7	breast:
12	chr12:57079048..57083970-chr12:57107938..57112602,6	K562	blood:
13	chr12:57111474..57114081-chr12:57143216..57146135,2	MCF-7	breast:
14	chr12:57113663..57115512-chr12:57124278..57127097,2	K562	blood:
15	chr12:57112603..57114130-chr12:57504633..57506166,2	K562	blood:
16	chr12:57112436..57114253-chr12:57144608..57146371,2	K562	blood:
17	chr12:57075341..57085478-chr12:57112447..57121011,58	MCF-7	breast:
18	chr12:57113713..57116326-chr12:57145534..57147437,2	MCF-7	breast:
19	chr12:57078475..57085183-chr12:57112918..57121559,38	K562	blood:

No data

Variant related genes	Relation type
NACA	TF binding region
NACA	CpG island
ENSG00000139641	chromatin interactions
ENSG00000076108	chromatin interactions
ENSG00000229117	chromatin interactions
ENSG00000135482	chromatin interactions
ENSG00000025423	chromatin interactions
ENSG00000198056	chromatin interactions
ENSG00000196531	chromatin interactions
ENSG00000207031	chromatin interactions
ENSG00000166888	chromatin interactions
ENSG00000110958	chromatin interactions
ENSG00000110955	chromatin interactions

Extended variants
information (count: 238 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:238 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141981954	chr12:57109861-57109862	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs576551678	chr12:57109874-57109875	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs374168332	chr12:57109877-57109878	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs145648145	chr12:57109902-57109903	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs200794039	chr12:57109903-57109904	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs2926747	chr12:57109931-57109932	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs199723539	chr12:57109935-57109936	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs541284931	chr12:57109948-57109949	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs371952741	chr12:57109949-57109950	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs111651575	chr12:57109961-57109962	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs149326268	chr12:57109979-57109980	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs372484247	chr12:57109993-57109994	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs183828032	chr12:57110000-57110001	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs368947398	chr12:57110008-57110009	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs530427863	chr12:57110014-57110015	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs187514929	chr12:57110023-57110024	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs570469875	chr12:57110037-57110038	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs534688195	chr12:57110096-57110097	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs546360887	chr12:57110101-57110102	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs375774655	chr12:57110107-57110108	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs201446430	chr12:57110141-57110142	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs191979856	chr12:57110168-57110169	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs557295893	chr12:57110213-57110214	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs369043787	chr12:57110215-57110216	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs372794179	chr12:57110229-57110230	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs539422172	chr12:57110231-57110232	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs144522448	chr12:57110236-57110237	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs558882061	chr12:57110253-57110254	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs375012026	chr12:57110312-57110313	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs577145616	chr12:57110313-57110314	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs201015074	chr12:57110364-57110365	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs369529375	chr12:57110387-57110388	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs76076193	chr12:57110442-57110443	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs200033251	chr12:57110445-57110446	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs541975611	chr12:57110487-57110488	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs184221111	chr12:57110501-57110502	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs371375736	chr12:57110519-57110520	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs371239609	chr12:57110534-57110535	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs373475432	chr12:57110554-57110555	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs202204935	chr12:57110577-57110578	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs564142402	chr12:57110614-57110615	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs528063005	chr12:57110620-57110621	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs376889735	chr12:57110654-57110655	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs546721072	chr12:57110721-57110722	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs61937760	chr12:57110723-57110724	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs568115356	chr12:57110724-57110725	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs187055425	chr12:57110785-57110786	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs372503104	chr12:57110793-57110794	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs199681422	chr12:57110807-57110808	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs539747122	chr12:57110825-57110826	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	20531469	CNVD
Rhabdomyosarcoma	16790082	CNVD
Renal cell carcinoma	18765545	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	21509527	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glycogen storage disease	18421352	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:423 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:57104000-57114600	Weak transcription	Fetal Brain Male	brain
2	chr12:57104600-57110200	Strong transcription	Fetal Stomach	stomach
3	chr12:57104600-57112600	Strong transcription	Fetal Intestine Large	intestine
4	chr12:57104600-57115000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr12:57104800-57110000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr12:57104800-57110000	Strong transcription	Brain Germinal Matrix	brain
7	chr12:57104800-57110000	Strong transcription	Stomach Smooth Muscle	stomach
8	chr12:57104800-57110000	Strong transcription	A549	lung
9	chr12:57104800-57110200	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr12:57104800-57110200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
11	chr12:57104800-57110200	Strong transcription	Placenta	Placenta
12	chr12:57104800-57110400	Strong transcription	Primary B cells from peripheral blood	blood
13	chr12:57104800-57110600	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr12:57104800-57110600	Strong transcription	Osteobl	bone
15	chr12:57104800-57111000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr12:57104800-57111200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr12:57104800-57111200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr12:57104800-57111200	Strong transcription	HUES6 Cell Line	embryonic stem cell
19	chr12:57104800-57111200	Strong transcription	HSMM	muscle
20	chr12:57104800-57111400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr12:57105000-57110000	Strong transcription	Primary B cells from cord blood	blood
22	chr12:57105000-57110200	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr12:57105000-57110200	Strong transcription	Dnd41	blood
24	chr12:57105000-57110400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
25	chr12:57105000-57110400	Strong transcription	Rectal Mucosa Donor 31	rectum
26	chr12:57105000-57110600	Strong transcription	Rectal Mucosa Donor 29	rectum
27	chr12:57105000-57110600	Strong transcription	HepG2	liver
28	chr12:57105000-57110600	Strong transcription	NHDF-Ad	bronchial
29	chr12:57105000-57110800	Strong transcription	Duodenum Mucosa	Duodenum
30	chr12:57105000-57111200	Strong transcription	HUES64 Cell Line	embryonic stem cell
31	chr12:57105000-57111400	Strong transcription	Primary T helper naive cells from peripheral blood	blood
32	chr12:57105000-57111600	Strong transcription	Cortex derived primary cultured neurospheres	brain
33	chr12:57105200-57110000	Strong transcription	Rectal Smooth Muscle	rectum
34	chr12:57105200-57110400	Strong transcription	H1 Cell Line	embryonic stem cell
35	chr12:57105200-57110400	Strong transcription	Sigmoid Colon	Sigmoid Colon
36	chr12:57105200-57110400	Strong transcription	HSMMtube	muscle
37	chr12:57105200-57110600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr12:57105200-57111200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr12:57105200-57112200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr12:57105800-57112200	Weak transcription	Fetal Heart	heart
41	chr12:57106000-57110200	Strong transcription	Primary hematopoietic stem cells	blood
42	chr12:57106000-57110600	Strong transcription	Brain Anterior Caudate	brain
43	chr12:57106000-57111000	Genic enhancers	Primary neutrophils fromperipheralblood	blood
44	chr12:57106200-57110000	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr12:57106200-57110200	Strong transcription	Primary T cells from cord blood	blood
46	chr12:57106200-57110200	Strong transcription	Fetal Brain Female	brain
47	chr12:57106200-57110200	Strong transcription	Fetal Lung	lung
48	chr12:57106200-57110200	Strong transcription	K562	blood
49	chr12:57106200-57110400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
50	chr12:57106400-57110200	Strong transcription	H9 Cell Line	embryonic stem cell

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