Variant report

Variant	nsv536748
Chromosome Location	chr3:143750590-144093775
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1173)
CpG islands
(count:367)
Chromatin interactive
region (count:95)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1173 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:143837779-143837958	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:143880755-143881509	HepG2	liver:	n/a	chr3:143881380-143881396
3	ATF1	chr3:143825901-143826204	K562	blood:	n/a	n/a
4	ATF1	chr3:143804936-143805091	K562	blood:	n/a	n/a
5	ATF2	chr3:143751298-143751934	GM12878	blood:	n/a	n/a
6	ATF2	chr3:143846788-143847440	GM12878	blood:	n/a	n/a
7	ATF2	chr3:143751294-143752090	GM12878	blood:	n/a	n/a
8	ATF2	chr3:143846465-143847491	GM12878	blood:	n/a	n/a
9	ATF2	chr3:144013376-144014503	GM12878	blood:	n/a	n/a
10	ATF2	chr3:144013394-144014434	GM12878	blood:	n/a	n/a
11	ATF2	chr3:143848494-143849137	GM12878	blood:	n/a	n/a
12	ATF2	chr3:143848478-143849143	GM12878	blood:	n/a	n/a
13	BACH1	chr3:143833588-143833943	K562	blood:	n/a	chr3:143833761-143833775
14	BACH1	chr3:143782248-143782473	K562	blood:	n/a	n/a
15	BACH1	chr3:143833582-143834019	H1-hESC	embryonic stem cell:	n/a	chr3:143833761-143833775
16	BACH1	chr3:143816071-143816361	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr3:144013966-144014424	GM12878	blood:	n/a	n/a
18	BATF	chr3:143846881-143847436	GM12878	blood:	n/a	n/a
19	BATF	chr3:144015695-144015975	GM12878	blood:	n/a	n/a
20	BATF	chr3:143828841-143829119	GM12878	blood:	n/a	n/a
21	BATF	chr3:144013492-144013785	GM12878	blood:	n/a	n/a
22	BATF	chr3:144013488-144013758	GM12878	blood:	n/a	n/a
23	BATF	chr3:143751468-143752084	GM12878	blood:	n/a	n/a
24	BATF	chr3:143848423-143849121	GM12878	blood:	n/a	n/a
25	BATF	chr3:144007957-144008191	GM12878	blood:	n/a	n/a
26	BATF	chr3:143751446-143751795	GM12878	blood:	n/a	n/a
27	BATF	chr3:143777624-143777852	GM12878	blood:	n/a	n/a
28	BATF	chr3:143848617-143849040	GM12878	blood:	n/a	n/a
29	BATF	chr3:144015688-144015947	GM12878	blood:	n/a	n/a
30	BATF	chr3:144013981-144014356	GM12878	blood:	n/a	n/a
31	BATF	chr3:143777619-143777840	GM12878	blood:	n/a	n/a
32	BCL11A	chr3:144013523-144013694	GM12878	blood:	n/a	n/a
33	BCL11A	chr3:143751375-143751790	GM12878	blood:	n/a	n/a
34	BCL11A	chr3:144014007-144014300	GM12878	blood:	n/a	n/a
35	BCL11A	chr3:144013972-144014361	GM12878	blood:	n/a	n/a
36	BCL11A	chr3:144015708-144016008	GM12878	blood:	n/a	n/a
37	BCL11A	chr3:144013477-144013896	GM12878	blood:	n/a	n/a
38	BCL11A	chr3:143848485-143849120	GM12878	blood:	n/a	n/a
39	BCL11A	chr3:143848674-143849066	GM12878	blood:	n/a	n/a
40	BCL3	chr3:144013975-144014412	GM12878	blood:	n/a	n/a
41	BCL3	chr3:143848594-143849036	GM12878	blood:	n/a	n/a
42	BCL3	chr3:144013510-144013878	GM12878	blood:	n/a	n/a
43	BCLAF1	chr3:144013925-144014474	GM12878	blood:	n/a	n/a
44	BCLAF1	chr3:144013974-144014372	GM12878	blood:	n/a	n/a
45	BCLAF1	chr3:144013490-144013836	GM12878	blood:	n/a	n/a
46	BCLAF1	chr3:143846960-143847480	GM12878	blood:	n/a	n/a
47	BCLAF1	chr3:143846949-143847398	GM12878	blood:	n/a	n/a
48	BHLHE40	chr3:144014030-144014341	GM12878	blood:	n/a	n/a
49	BHLHE40	chr3:143828859-143828869	GM12878	blood:	n/a	n/a
50	BHLHE40	chr3:143825952-143826076	K562	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:143815849-143815899	HEEpiC	esophagus:	n/a
2	chr3:143815849-143815899	HEEpiC	esophagus:	n/a
3	chr3:143773022-143773072	GM19239	blood:	n/a
4	chr3:143773022-143773072	Hela-S3	cervix:	n/a
5	chr3:143847318-143847368	HRCEpiC	kidney:	n/a
6	chr3:143815849-143815899	HCPEpiC	choroid plexus:	n/a
7	chr3:143773022-143773072	HEEpiC	esophagus:	n/a
8	chr3:143773022-143773072	ECC-1	luminal epithelium:	n/a
9	chr3:143847318-143847368	HNPCEpiC	eye:	n/a
10	chr3:143861209-143861259	U87	brain:	n/a
11	chr3:143815849-143815899	NT2-D1	testis:	n/a
12	chr3:143815849-143815899	BJ	skin:	n/a
13	chr3:143861209-143861259	CMK	blood:	n/a
14	chr3:144064632-144064682	Hepatocyte	liver:	n/a
15	chr3:143993048-143993098	HAEpiC	amniotic membrane:	n/a
16	chr3:144064632-144064682	HEK293	kidney:	embryo
17	chr3:143861209-143861259	PANC-1	pancreas:	n/a
18	chr3:143861209-143861259	HUVEC	blood vessel:	n/a
19	chr3:143773022-143773072	BE2_C	brain:	n/a
20	chr3:143861209-143861259	K562	blood:	n/a
21	chr3:143861209-143861259	Hepatocyte	liver:	n/a
22	chr3:143815849-143815899	HCT-116	colon:	n/a
23	chr3:143773022-143773072	LNCaP	prostate:	n/a
24	chr3:143861209-143861259	AG04449	skin:	fetal
25	chr3:144064632-144064682	RPTEC	kidney:	n/a
26	chr3:143847318-143847368	GM12878	blood:	n/a
27	chr3:143815849-143815899	ECC-1	luminal epithelium:	n/a
28	chr3:143993048-143993098	SK-N-SH	brain:	n/a
29	chr3:143815849-143815899	T-47D	breast:	n/a
30	chr3:143847318-143847368	MCF10A-Er-Src	breast:	n/a
31	chr3:143861209-143861259	NH-A	brain:	n/a
32	chr3:143847318-143847368	AG04449	skin:	fetal
33	chr3:143773022-143773072	AG10803	skin:	n/a
34	chr3:143993048-143993098	ECC-1	luminal epithelium:	n/a
35	chr3:143773022-143773072	HMEC	breast:	n/a
36	chr3:143847318-143847368	HEEpiC	esophagus:	n/a
37	chr3:143773022-143773072	IMR90	lung:	fetal
38	chr3:143815849-143815899	Hepatocyte	liver:	n/a
39	chr3:143773022-143773072	AG09319	gingival:	n/a
40	chr3:143773022-143773072	MCF10A-Er-Src	breast:	n/a
41	chr3:143847318-143847368	NHBE	bronchial:	n/a
42	chr3:143773022-143773072	AoSMC	blood vessel:	n/a
43	chr3:143815849-143815899	LNCaP	prostate:	n/a
44	chr3:143815849-143815899	GM06990	blood:	n/a
45	chr3:144064632-144064682	GM12878	blood:	n/a
46	chr3:143861209-143861259	GM12891	blood:	n/a
47	chr3:143847318-143847368	HPAEpiC	pulmonary alveolar:	n/a
48	chr3:143847318-143847368	AG04450	lung:	fetal
49	chr3:144064632-144064682	SAEC	small airway:	n/a
50	chr3:143993048-143993098	GM19239	blood:	n/a

(count:95 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:143738952..143741203-chr3:143757677..143760166,2	K562	blood:
2	chr3:143902901..143904761-chr3:143930558..143932653,2	MCF-7	breast:
3	chr3:61879348..61880969-chr3:143831622..143834006,2	MCF-7	breast:
4	chr3:143690019..143692645-chr3:143838592..143840602,2	MCF-7	breast:
5	chr3:143962916..143965594-chr3:143970666..143973506,3	MCF-7	breast:
6	chr12:53342265..53345092-chr3:144025098..144026936,2	MCF-7	breast:
7	chr3:144081380..144083879-chr3:144086232..144088333,2	MCF-7	breast:
8	chr3:144026496..144028084-chr3:144029746..144032575,2	MCF-7	breast:
9	chr3:144047302..144050208-chr3:144050986..144053451,2	K562	blood:
10	chr3:143890771..143894320-chr3:143898037..143901332,4	MCF-7	breast:
11	chr3:143852522..143855348-chr3:143858842..143861138,3	K562	blood:
12	chr3:143851188..143852094-chr3:143864087..143864848,2	MCF-7	breast:
13	chr3:143862145..143864475-chr3:143867360..143869304,2	K562	blood:
14	chr17:56707384..56710273-chr3:144036844..144039092,2	MCF-7	breast:
15	chr3:143695787..143698743-chr3:143748690..143750623,2	K562	blood:
16	chr3:143691185..143693513-chr3:143753379..143757056,4	K562	blood:
17	chr3:144026496..144028084-chr3:144029746..144032575,2	MCF-7	breast:
18	chr3:144012906..144014762-chr3:144016607..144019319,2	MCF-7	breast:
19	chr3:143882905..143885862-chr3:143887105..143889283,2	MCF-7	breast:
20	chr3:143976073..143978906-chr3:143983000..143985910,2	K562	blood:
21	chr3:143796834..143798439-chr3:143800651..143803493,2	MCF-7	breast:
22	chr3:143862145..143864475-chr3:143867360..143869304,2	K562	blood:
23	chr3:143886285..143888723-chr3:143892668..143894323,2	MCF-7	breast:
24	chr3:143691660..143693819-chr3:143749390..143751608,2	K562	blood:
25	chr3:143802113..143803732-chr3:143807237..143809098,2	K562	blood:
26	chr3:143797616..143799320-chr3:143802598..143805481,2	MCF-7	breast:
27	chr3:143851188..143852094-chr3:143864087..143864848,2	MCF-7	breast:
28	chr3:144081380..144083879-chr3:144086232..144088333,2	MCF-7	breast:
29	chr3:143985749..143987878-chr3:143995682..143998153,2	MCF-7	breast:
30	chr3:143852522..143854486-chr3:143858842..143860873,2	K562	blood:
31	chr3:143691448..143693867-chr3:143753525..143755680,2	K562	blood:
32	chr3:143819810..143821704-chr3:143822907..143824829,2	K562	blood:
33	chr3:143872336..143874000-chr3:143882246..143884179,2	K562	blood:
34	chr3:143872336..143874000-chr3:143882246..143884179,2	K562	blood:
35	chr3:143690008..143692264-chr3:143879594..143881502,2	MCF-7	breast:
36	chr3:143804757..143807049-chr3:143809436..143811343,2	MCF-7	breast:
37	chr3:143690072..143692415-chr3:143771127..143773744,2	MCF-7	breast:
38	chr3:143689363..143691415-chr3:143803802..143806594,3	MCF-7	breast:
39	chr3:143900814..143902970-chr3:143905127..143907243,2	K562	blood:
40	chr12:53061288..53061963-chr3:143990811..143991640,2	MCF-7	breast:
41	chr3:143892804..143894519-chr3:143897127..143900073,2	K562	blood:
42	chr3:143892804..143894519-chr3:143897127..143900073,2	K562	blood:
43	chr3:143970717..143972446-chr3:143972808..143975131,2	K562	blood:
44	chr3:143717685..143719346-chr3:143782583..143784716,2	K562	blood:
45	chr3:143689173..143691180-chr3:143749985..143751944,2	K562	blood:
46	chr3:144012906..144014762-chr3:144016607..144019319,2	MCF-7	breast:
47	chr3:143694158..143694846-chr3:143996996..143997942,2	MCF-7	breast:
48	chr3:143690687..143692253-chr3:144007125..144008743,2	MCF-7	breast:
49	chr3:143797616..143799320-chr3:143802598..143805481,2	MCF-7	breast:
50	chr3:143892267..143895225-chr3:144092173..144094543,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHST2-5	chr3:143753460-143753522	XLOC_002851
2	lnc-CHST2-5	chr3:143755567-143755742	XLOC_002851
3	lnc-C3orf58-1	chr3:143936262-143938475	NONHSAT092535

No data

Variant related genes	Relation type
RNA5SP144	TF binding region
RNA5SP144	CpG island
ENSG00000170421	chromatin interactions
ENSG00000181744	chromatin interactions
ENSG00000111057	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000269694	chromatin interactions
ENSG00000222778	chromatin interactions

Extended variants
information (count: 9393 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:9393 , 50 per page) page: 1 2 3 4 5 6 7 ... 188

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573742061	chr3:143750620-143750621	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs534617723	chr3:143750727-143750728	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs552846739	chr3:143750746-143750747	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs572148645	chr3:143750765-143750766	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs193122539	chr3:143750779-143750780	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs557702193	chr3:143750814-143750815	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs576474639	chr3:143750830-143750831	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs543856692	chr3:143750854-143750855	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs76569427	chr3:143750887-143750888	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs529485192	chr3:143751025-143751026	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs541399158	chr3:143751031-143751032	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs560070278	chr3:143751052-143751053	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs559949117	chr3:143751093-143751094	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs184467111	chr3:143751144-143751145	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs367813578	chr3:143751213-143751214	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs150137594	chr3:143751230-143751231	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs569636893	chr3:143751251-143751252	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs530531573	chr3:143751303-143751304	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs531631333	chr3:143751339-143751340	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs550234733	chr3:143751448-143751449	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs73874109	chr3:143751454-143751455	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs534806884	chr3:143751590-143751591	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs552884101	chr3:143751598-143751599	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs150557059	chr3:143751626-143751627	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs538510366	chr3:143751627-143751628	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs557738828	chr3:143751649-143751650	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs139654305	chr3:143751695-143751696	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs543596835	chr3:143751719-143751720	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs535590898	chr3:143751749-143751750	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs188477824	chr3:143751796-143751797	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs181278359	chr3:143751810-143751811	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs147599975	chr3:143751831-143751832	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs547827548	chr3:143751836-143751837	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs149735865	chr3:143751866-143751867	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs533685538	chr3:143751891-143751892	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs545678774	chr3:143751956-143751957	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs116579439	chr3:143751964-143751965	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs530525664	chr3:143751968-143751969	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs184964916	chr3:143752032-143752033	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs7639366	chr3:143752034-143752035	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs113064504	chr3:143752086-143752087	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs113590736	chr3:143752098-143752099	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs376712067	chr3:143752154-143752155	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs367629367	chr3:143752188-143752189	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs546404585	chr3:143752204-143752205	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs370985818	chr3:143752205-143752206	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs528825017	chr3:143752226-143752227	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs571068212	chr3:143752251-143752252	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs528308490	chr3:143752275-143752276	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs189513687	chr3:143752298-143752299	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	21509527	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1229 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143747600-143750800	Weak transcription	Ovary	ovary
2	chr3:143748600-143751600	Weak transcription	Primary B cells from peripheral blood	blood
3	chr3:143749200-143750800	Weak transcription	Brain Angular Gyrus	brain
4	chr3:143749800-143750800	Enhancers	GM12878-XiMat	blood
5	chr3:143750000-143750600	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr3:143750000-143751000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr3:143750000-143754200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr3:143750200-143750600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr3:143750200-143750600	Flanking Active TSS	Brain Hippocampus Middle	brain
10	chr3:143750200-143750600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
11	chr3:143750200-143750600	Enhancers	Stomach Smooth Muscle	stomach
12	chr3:143750200-143750800	Enhancers	Brain Substantia Nigra	brain
13	chr3:143750200-143751000	Enhancers	H1 Cell Line	embryonic stem cell
14	chr3:143750200-143751000	Active TSS	Brain Cingulate Gyrus	brain
15	chr3:143750200-143751200	Enhancers	NHEK	skin
16	chr3:143750200-143753600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
17	chr3:143750400-143750600	Flanking Active TSS	Brain Anterior Caudate	brain
18	chr3:143750400-143750600	Enhancers	Duodenum Smooth Muscle	Duodenum
19	chr3:143750400-143750800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr3:143750400-143750800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr3:143750400-143750800	Enhancers	HSMM	muscle
22	chr3:143750400-143751000	Enhancers	HSMMtube	muscle
23	chr3:143750400-143751800	Enhancers	Muscle Satellite Cultured Cells	--
24	chr3:143750400-143752600	Enhancers	Colon Smooth Muscle	Colon
25	chr3:143750400-143753200	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr3:143750600-143750800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr3:143750600-143750800	Active TSS	Brain Anterior Caudate	brain
28	chr3:143750600-143750800	Enhancers	Brain Hippocampus Middle	brain
29	chr3:143750600-143750800	Active TSS	Brain Inferior Temporal Lobe	brain
30	chr3:143750600-143751000	Enhancers	Liver	Liver
31	chr3:143750600-143751000	Active TSS	Stomach Smooth Muscle	stomach
32	chr3:143750600-143751200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr3:143750800-143751000	Flanking Active TSS	Brain Hippocampus Middle	brain
34	chr3:143750800-143751000	Enhancers	Sigmoid Colon	Sigmoid Colon
35	chr3:143750800-143751200	Weak transcription	Brain Substantia Nigra	brain
36	chr3:143750800-143751200	Enhancers	Esophagus	oesophagus
37	chr3:143750800-143751200	Active TSS	Right Atrium	heart
38	chr3:143750800-143751200	Flanking Active TSS	HSMM	muscle
39	chr3:143750800-143751200	Enhancers	NH-A	brain
40	chr3:143750800-143751200	Enhancers	NHLF	lung
41	chr3:143750800-143751600	Active TSS	Brain Angular Gyrus	brain
42	chr3:143750800-143751800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr3:143750800-143751800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr3:143750800-143751800	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr3:143750800-143751800	Active TSS	Osteobl	bone
46	chr3:143750800-143752000	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr3:143750800-143752600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr3:143750800-143752600	Flanking Active TSS	GM12878-XiMat	blood
49	chr3:143750800-143752800	Enhancers	Rectal Smooth Muscle	rectum
50	chr3:143750800-143753200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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