Variant report

Variant	nsv899290
Chromosome Location	chr12:74666737-74729489
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:475)
CpG islands
(count:549)
Chromatin interactive
region (count:38)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:475 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:74686394-74686740	K562	blood:	n/a	n/a
2	ARID3A	chr12:74677511-74677734	K562	blood:	n/a	n/a
3	ATF1	chr12:74706672-74706735	K562	blood:	n/a	n/a
4	ATF1	chr12:74686375-74686953	K562	blood:	n/a	n/a
5	BHLHE40	chr12:74686194-74687073	K562	blood:	n/a	n/a
6	BHLHE40	chr12:74687322-74688058	K562	blood:	n/a	n/a
7	CBX3	chr12:74686301-74686730	K562	blood:	n/a	n/a
8	CBX3	chr12:74687157-74687922	K562	blood:	n/a	n/a
9	CBX3	chr12:74686218-74687007	K562	blood:	n/a	n/a
10	CCNT2	chr12:74686228-74686909	K562	blood:	n/a	chr12:74686489-74686509
11	CEBPB	chr12:74725661-74726101	A549	lung:	n/a	n/a
12	CEBPB	chr12:74728414-74729029	HCT-116	colon:	n/a	n/a
13	CEBPB	chr12:74686227-74686696	K562	blood:	n/a	n/a
14	CEBPB	chr12:74725734-74726056	IMR90	lung:	n/a	n/a
15	CEBPB	chr12:74717021-74717301	K562	blood:	n/a	chr12:74717187-74717200 chr12:74717187-74717200 chr12:74717189-74717200 chr12:74717243-74717256
16	CEBPB	chr12:74718452-74718672	K562	blood:	n/a	chr12:74718562-74718573
17	CEBPB	chr12:74718420-74718696	HepG2	liver:	n/a	chr12:74718562-74718573
18	CEBPB	chr12:74725757-74726048	HepG2	liver:	n/a	n/a
19	CEBPB	chr12:74686352-74686893	K562	blood:	n/a	n/a
20	CEBPB	chr12:74679616-74679818	A549	lung:	n/a	n/a
21	CEBPB	chr12:74725768-74726034	MCF-7	breast:	n/a	n/a
22	CEBPB	chr12:74680258-74680372	K562	blood:	n/a	n/a
23	CEBPB	chr12:74728409-74729025	HCT-116	colon:	n/a	n/a
24	CEBPD	chr12:74686172-74686749	K562	blood:	n/a	n/a
25	CHD2	chr12:74687474-74687667	K562	blood:	n/a	n/a
26	CHD2	chr12:74686188-74686982	K562	blood:	n/a	n/a
27	CHD2	chr12:74687891-74688044	K562	blood:	n/a	n/a
28	CTCF	chr12:74710774-74711156	H1-hESC	embryonic stem cell:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
29	CTCF	chr12:74710860-74711010	SK-N-SH_RA	brain:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
30	CTCF	chr12:74710894-74711045	Kidney_OC	kidney:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
31	CTCF	chr12:74710940-74711090	HUVEC	blood vessel:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
32	CTCF	chr12:74710840-74710990	HCM	heart:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
33	CTCF	chr12:74710940-74711090	HL-60	blood:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
34	CTCF	chr12:74710860-74711010	HEEpiC	esophagus:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
35	CTCF	chr12:74710645-74711203	MCF-7	breast:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
36	CTCF	chr12:74710740-74710890	GM12872	blood:	n/a	n/a
37	CTCF	chr12:74710832-74711122	Gliobla	brain:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
38	CTCF	chr12:74710880-74711030	RPTEC	kidney:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
39	CTCF	chr12:74710900-74711050	HRPEpiC	eye:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
40	CTCF	chr12:74710820-74710970	HAc	cerebellar:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
41	CTCF	chr12:74710902-74711097	MCF-7	breast:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
42	CTCF	chr12:74710880-74711030	HRE	kidney:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
43	CTCF	chr12:74710714-74711285	HCT-116	colon:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
44	CTCF	chr12:74710837-74711104	K562	blood:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
45	CTCF	chr12:74710864-74711091	SK-N-SH_RA	brain:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
46	CTCF	chr12:74710904-74711030	GM13977	blood:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
47	CTCF	chr12:74710940-74711090	BE2_C	brain:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
48	CTCF	chr12:74710880-74711030	HCPEpiC	choroid plexus:	n/a	chr12:74710949-74710967 chr12:74710944-74710965
49	CTCF	chr12:74710949-74710952	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr12:74710980-74711130	HCT-116	colon:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:74686430-74686480	AG09309	skin:	n/a
2	chr12:74687404-74687454	GM19239	blood:	n/a
3	chr12:74686411-74686461	RPTEC	kidney:	n/a
4	chr12:74687404-74687454	SK-N-MC	brain:	n/a
5	chr12:74686282-74686332	HEEpiC	esophagus:	n/a
6	chr12:74686282-74686332	GM12878	blood:	n/a
7	chr12:74687807-74687857	HCM	heart:	n/a
8	chr12:74687404-74687454	Hela-S3	cervix:	n/a
9	chr12:74688000-74688050	PANC-1	pancreas:	n/a
10	chr12:74686411-74686461	Caco-2	colon:	n/a
11	chr12:74686423-74686473	Hepatocyte	liver:	n/a
12	chr12:74686367-74686417	ProgFib	skin:	n/a
13	chr12:74686367-74686417	HRCEpiC	kidney:	n/a
14	chr12:74686282-74686332	SK-N-SH_RA	brain:	n/a
15	chr12:74687807-74687857	ProgFib	skin:	n/a
16	chr12:74687807-74687857	HCT-116	colon:	n/a
17	chr12:74686423-74686473	SAEC	small airway:	n/a
18	chr12:74687807-74687857	BJ	skin:	n/a
19	chr12:74686411-74686461	ProgFib	skin:	n/a
20	chr12:74686430-74686480	HRPEpiC	eye:	n/a
21	chr12:74688000-74688050	SAEC	small airway:	n/a
22	chr12:74686430-74686480	NH-A	brain:	n/a
23	chr12:74686367-74686417	HUVEC	blood vessel:	n/a
24	chr12:74686282-74686332	RPTEC	kidney:	n/a
25	chr12:74687404-74687454	CMK	blood:	n/a
26	chr12:74686430-74686480	HRE	kidney:	n/a
27	chr12:74686411-74686461	HepG2	liver:	n/a
28	chr12:74687807-74687857	GM06990	blood:	n/a
29	chr12:74687404-74687454	HEK293	kidney:	embryo
30	chr12:74687404-74687454	Caco-2	colon:	n/a
31	chr12:74687807-74687857	HCF	heart:	n/a
32	chr12:74686430-74686480	SAEC	small airway:	n/a
33	chr12:74687852-74687902	GM12878	blood:	n/a
34	chr12:74687852-74687902	CMK	blood:	n/a
35	chr12:74686430-74686480	AG04450	lung:	fetal
36	chr12:74686430-74686480	SK-N-MC	brain:	n/a
37	chr12:74687852-74687902	HepG2	liver:	n/a
38	chr12:74687404-74687454	AG09319	gingival:	n/a
39	chr12:74686430-74686480	CMK	blood:	n/a
40	chr12:74686411-74686461	HPAEpiC	pulmonary alveolar:	n/a
41	chr12:74686430-74686480	HCT-116	colon:	n/a
42	chr12:74686367-74686417	NH-A	brain:	n/a
43	chr12:74686411-74686461	HNPCEpiC	eye:	n/a
44	chr12:74686411-74686461	MCF10A-Er-Src	breast:	n/a
45	chr12:74686423-74686473	HEEpiC	esophagus:	n/a
46	chr12:74686367-74686417	K562	blood:	n/a
47	chr12:74686282-74686332	GM12892	blood:	n/a
48	chr12:74687807-74687857	HCPEpiC	choroid plexus:	n/a
49	chr12:74686282-74686332	AG04450	lung:	fetal
50	chr12:74686430-74686480	T-47D	breast:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:74722908..74725146-chr12:74726519..74728134,2	K562	blood:
2	chr12:74683373..74686280-chr12:74686483..74688021,2	K562	blood:
3	chr12:74682181..74684758-chr12:74690974..74692662,2	MCF-7	breast:
4	chr12:74697259..74699490-chr12:74701397..74704397,3	K562	blood:
5	chr12:74700385..74702258-chr12:74705662..74707341,2	K562	blood:
6	chr12:74710734..74711407-chr12:74759142..74759810,2	MCF-7	breast:
7	chr12:74563726..74565313-chr12:74683248..74684953,2	K562	blood:
8	chr12:74723847..74726680-chr12:74730834..74733309,2	MCF-7	breast:
9	chr12:74686333..74689178-chr12:74690372..74695495,6	K562	blood:
10	chr12:74505546..74506081-chr12:74710850..74711455,2	MCF-7	breast:
11	chr12:74644729..74646901-chr12:74673133..74675574,2	K562	blood:
12	chr12:74665740..74669751-chr12:74671344..74674608,3	K562	blood:
13	chr12:74696546..74698313-chr12:74705755..74707980,2	K562	blood:
14	chr12:74694041..74696981-chr12:74709470..74713007,3	K562	blood:
15	chr12:74682181..74684758-chr12:74690974..74692662,2	MCF-7	breast:
16	chr12:74690922..74693086-chr12:74695420..74697032,3	K562	blood:
17	chr12:74505235..74505774-chr12:74710528..74711393,3	K562	blood:
18	chr12:74415312..74416230-chr12:74710631..74711359,2	MCF-7	breast:
19	chr12:74683373..74686280-chr12:74686483..74688021,2	K562	blood:
20	chr12:74694041..74696981-chr12:74709470..74713007,3	K562	blood:
21	chr12:74700385..74702258-chr12:74705662..74707341,2	K562	blood:
22	chr12:74636496..74638215-chr12:74687391..74689120,2	K562	blood:
23	chr12:74717186..74718789-chr12:74720353..74721970,2	K562	blood:
24	chr12:74695518..74698139-chr12:74698904..74700700,2	MCF-7	breast:
25	chr12:74666319..74668697-chr12:74685247..74688031,2	K562	blood:
26	chr12:74683740..74685933-chr12:74788608..74790315,2	K562	blood:
27	chr12:74687125..74689371-chr12:74929648..74931476,2	K562	blood:
28	chr12:74697259..74699490-chr12:74701397..74704397,3	K562	blood:
29	chr12:74690922..74693086-chr12:74695420..74697032,3	K562	blood:
30	chr12:74685273..74687304-chrX:26574250..26577248,2	K562	blood:
31	chr12:74505191..74505755-chr12:74710574..74711440,3	MCF-7	breast:
32	chr12:74722908..74725146-chr12:74726519..74728134,2	K562	blood:
33	chr12:74686465..74688529-chr12:74932040..74934610,2	K562	blood:
34	chr12:74728722..74730831-chr12:74734863..74737720,2	K562	blood:
35	chr12:74685342..74687615-chr12:74688335..74689861,2	K562	blood:
36	chr12:74717186..74718789-chr12:74720353..74721970,2	K562	blood:
37	chr12:74695518..74698139-chr12:74698904..74700700,2	MCF-7	breast:
38	chr12:74696546..74698313-chr12:74705755..74707980,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNC2-2	chr12:74679478-74679726	ENSG00000251138
2	lnc-KCNC2-2	chr12:74715315-74715474	ENSG00000251138
3	lnc-KCNC2-3	chr12:74677374-74677449	ENSG00000257183.1
4	lnc-KCNC2-2	chr12:74679640-74679726	ENSG00000251138
5	lnc-KCNC2-2	chr12:74686095-74686314	ENSG00000251138
6	lnc-KCNC2-2	chr12:74678816-74678873	ENSG00000251138
7	lnc-ATXN7L3B-5	chr12:74668732-74669011	NONHSAT029501
8	lnc-KCNC2-2	chr12:74700338-74700449	ENSG00000251138

No data

Variant related genes	Relation type
ENSG00000257183	TF binding region
ENSG00000257113	TF binding region
ENSG00000257364	TF binding region
ENSG00000251138	TF binding region
ENSG00000257183	CpG island
ENSG00000257113	CpG island
ENSG00000257364	CpG island
ENSG00000251138	CpG island
ENSG00000230265	chromatin interactions
ENSG00000257364	chromatin interactions
ENSG00000257386	chromatin interactions
ENSG00000258320	chromatin interactions
ENSG00000257113	chromatin interactions
ENSG00000259849	chromatin interactions
ENSG00000251138	chromatin interactions
RRAS	miRNA target sites
HOXC8	miRNA target sites
DNMT1	miRNA target sites
SNAPIN	miRNA target sites
DYNLL2	miRNA target sites
PROSC	miRNA target sites

Extended variants
information (count: 1863 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1863 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7971189	chr12:74666737-74666738	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs199596658	chr12:74666791-74666792	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs572324441	chr12:74666881-74666882	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs539841182	chr12:74666952-74666953	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs556309128	chr12:74666970-74666971	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs576310658	chr12:74667002-74667003	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs4601862	chr12:74667003-74667004	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs150038343	chr12:74667020-74667021	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs572317355	chr12:74667052-74667053	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs66504708	chr12:74667066-74667067	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs145298356	chr12:74667091-74667092	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs532137337	chr12:74667107-74667108	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs545769265	chr12:74667121-74667122	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs545708313	chr12:74667133-74667134	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs189953483	chr12:74667137-74667138	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs529892194	chr12:74667197-74667198	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs562508311	chr12:74667206-74667207	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs531633733	chr12:74667245-74667246	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs180802384	chr12:74667272-74667273	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs568218877	chr12:74667292-74667293	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs73351767	chr12:74667293-74667294	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs199543443	chr12:74667323-74667324	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs573593266	chr12:74667338-74667339	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs536166951	chr12:74667344-74667345	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs549543872	chr12:74667425-74667426	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs36054289	chr12:74667480-74667481	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs570899598	chr12:74667515-74667516	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs78113728	chr12:74667564-74667565	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs556521306	chr12:74667625-74667626	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs569720175	chr12:74667688-74667689	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs376343791	chr12:74667704-74667705	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs73351769	chr12:74667706-74667707	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs115976725	chr12:74667743-74667744	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs541592942	chr12:74667753-74667754	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs149222454	chr12:74667800-74667801	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs576862429	chr12:74667868-74667869	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs545626853	chr12:74667893-74667894	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs114634324	chr12:74667908-74667909	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs541439809	chr12:74667934-74667935	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs542109721	chr12:74667935-74667936	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs189311351	chr12:74667938-74667939	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs531662336	chr12:74667993-74667994	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs527616181	chr12:74668003-74668004	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs547552590	chr12:74668036-74668037	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs564381014	chr12:74668059-74668060	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs143411269	chr12:74668071-74668072	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs533421092	chr12:74668138-74668139	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs146871498	chr12:74668181-74668182	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs569683114	chr12:74668246-74668247	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs535480008	chr12:74668336-74668337	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	20409316	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:74636600-74678000	Weak transcription	K562	blood
2	chr12:74674000-74674800	Enhancers	Liver	Liver
3	chr12:74674800-74676200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr12:74675000-74676000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:74675200-74676000	Enhancers	HMEC	breast
6	chr12:74676000-74679000	Weak transcription	HMEC	breast
7	chr12:74676200-74679200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr12:74678000-74678600	Genic enhancers	K562	blood
9	chr12:74678600-74678800	Strong transcription	K562	blood
10	chr12:74678800-74679400	Weak transcription	K562	blood
11	chr12:74679000-74679200	Enhancers	HMEC	breast
12	chr12:74679000-74679400	Enhancers	Placenta	Placenta
13	chr12:74679200-74679600	Weak transcription	HMEC	breast
14	chr12:74679200-74680000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr12:74679200-74680000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr12:74679200-74681400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr12:74679400-74680400	Enhancers	K562	blood
18	chr12:74679600-74680200	Enhancers	HMEC	breast
19	chr12:74679800-74680200	Enhancers	NHEK	skin
20	chr12:74680000-74680200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr12:74680000-74681000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr12:74680400-74680800	Weak transcription	K562	blood
23	chr12:74680800-74681000	Enhancers	K562	blood
24	chr12:74681000-74681200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr12:74681000-74681200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr12:74681000-74683600	Weak transcription	K562	blood
27	chr12:74681400-74690800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr12:74681800-74682200	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr12:74681800-74683000	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr12:74682000-74682400	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr12:74682400-74682800	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr12:74683000-74685600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr12:74683600-74684400	Enhancers	K562	blood
34	chr12:74684400-74684800	Flanking Active TSS	K562	blood
35	chr12:74684800-74686800	Active TSS	K562	blood
36	chr12:74685600-74688000	Active TSS	ES-I3 Cell Line	embryonic stem cell
37	chr12:74686000-74687600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr12:74686200-74687000	Enhancers	H1 Cell Line	embryonic stem cell
39	chr12:74686200-74688000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr12:74686400-74687800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr12:74686600-74687000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr12:74686600-74687000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr12:74686600-74689000	Weak transcription	Right Atrium	heart
44	chr12:74686800-74688000	Flanking Active TSS	K562	blood
45	chr12:74687600-74687800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr12:74687800-74688000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr12:74688000-74688200	Active TSS	K562	blood
48	chr12:74688200-74691800	Weak transcription	K562	blood
49	chr12:74691800-74692200	Enhancers	K562	blood
50	chr12:74703600-74704000	Enhancers	Fetal Heart	heart

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