Variant report

Variant	esv3445096
Chromosome Location	chr1:75933216-76126980
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1441)
CpG islands
(count:1468)
Chromatin interactive
region (count:79)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1441 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:76082080-76082152	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:76105897-76106242	K562	blood:	n/a	n/a
3	ARID3A	chr1:75957729-75958079	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:75967127-75967618	K562	blood:	n/a	n/a
5	ARID3A	chr1:76043585-76043706	K562	blood:	n/a	n/a
6	ARID3A	chr1:75941380-75941568	K562	blood:	n/a	n/a
7	ARID3A	chr1:75968543-75968797	K562	blood:	n/a	n/a
8	ARID3A	chr1:75937012-75938909	K562	blood:	n/a	n/a
9	ARID3A	chr1:75987556-75987697	K562	blood:	n/a	n/a
10	ARID3A	chr1:75936261-75936335	K562	blood:	n/a	n/a
11	ATF1	chr1:75968529-75969161	K562	blood:	n/a	n/a
12	ATF1	chr1:76105885-76106222	K562	blood:	n/a	n/a
13	ATF1	chr1:76080039-76080344	K562	blood:	n/a	n/a
14	ATF1	chr1:76109354-76109542	K562	blood:	n/a	n/a
15	ATF1	chr1:75938131-75938751	K562	blood:	n/a	n/a
16	ATF1	chr1:75986599-75986936	K562	blood:	n/a	n/a
17	ATF1	chr1:76082531-76082931	K562	blood:	n/a	n/a
18	ATF2	chr1:76095599-76095993	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr1:75933751-75933871	K562	blood:	n/a	n/a
20	BACH1	chr1:76082259-76082774	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr1:75986272-75986985	K562	blood:	n/a	n/a
22	BACH1	chr1:75967313-75967571	K562	blood:	n/a	n/a
23	BACH1	chr1:75935646-75935837	K562	blood:	n/a	n/a
24	BACH1	chr1:76003667-76003673	K562	blood:	n/a	n/a
25	BACH1	chr1:76080097-76080757	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr1:75994248-75994466	K562	blood:	n/a	n/a
27	BACH1	chr1:75986537-75986787	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr1:76049181-76049309	H1-hESC	embryonic stem cell:	n/a	n/a
29	BCL3	chr1:76050161-76050475	GM12878	blood:	n/a	n/a
30	BHLHE40	chr1:76105917-76106244	K562	blood:	n/a	n/a
31	BHLHE40	chr1:75993618-75993712	K562	blood:	n/a	n/a
32	BHLHE40	chr1:76105293-76105429	K562	blood:	n/a	n/a
33	BHLHE40	chr1:76047972-76048172	K562	blood:	n/a	n/a
34	BHLHE40	chr1:76107180-76107438	K562	blood:	n/a	n/a
35	BHLHE40	chr1:76049346-76049464	GM12878	blood:	n/a	n/a
36	BHLHE40	chr1:75937875-75938713	K562	blood:	n/a	n/a
37	BHLHE40	chr1:76007429-76007491	K562	blood:	n/a	n/a
38	BHLHE40	chr1:75983321-75983377	HepG2	liver:	n/a	n/a
39	BHLHE40	chr1:76098240-76098424	GM12878	blood:	n/a	n/a
40	BHLHE40	chr1:76082516-76082778	K562	blood:	n/a	n/a
41	BHLHE40	chr1:75936244-75936716	K562	blood:	n/a	n/a
42	CBX3	chr1:75986473-75986873	K562	blood:	n/a	n/a
43	CBX3	chr1:76112759-76113226	K562	blood:	n/a	n/a
44	CBX3	chr1:75950547-75950751	K562	blood:	n/a	n/a
45	CBX3	chr1:75950247-75950507	K562	blood:	n/a	n/a
46	CBX3	chr1:75968883-75969316	K562	blood:	n/a	n/a
47	CCNT2	chr1:75967339-75967627	K562	blood:	n/a	n/a
48	CCNT2	chr1:75938082-75938574	K562	blood:	n/a	n/a
49	CCNT2	chr1:76105959-76106219	K562	blood:	n/a	n/a
50	CCNT2	chr1:76081434-76081868	K562	blood:	n/a	n/a

(count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:76081962-76082012	HUVEC	blood vessel:	n/a
2	chr1:76076088-76076138	H1-hESC	embryonic stem cell:	embryo
3	chr1:76081379-76081429	HCM	heart:	n/a
4	chr1:76081408-76081458	BJ	skin:	n/a
5	chr1:76081962-76082012	HUVEC	blood vessel:	n/a
6	chr1:76076088-76076138	H1-hESC	embryonic stem cell:	embryo
7	chr1:76081379-76081429	HCM	heart:	n/a
8	chr1:76081408-76081458	BJ	skin:	n/a
9	chr1:76085151-76085201	AG10803	skin:	n/a
10	chr1:76095838-76095888	CMK	blood:	n/a
11	chr1:76081272-76081322	HCPEpiC	choroid plexus:	n/a
12	chr1:76082568-76082618	NH-A	brain:	n/a
13	chr1:76081408-76081458	HRPEpiC	eye:	n/a
14	chr1:76076088-76076138	LNCaP	prostate:	n/a
15	chr1:76079833-76079883	K562	blood:	n/a
16	chr1:76081379-76081429	SK-N-MC	brain:	n/a
17	chr1:76082888-76082938	HEEpiC	esophagus:	n/a
18	chr1:76078176-76078226	NHDF-neo	bronchial:	n/a
19	chr1:76080459-76080509	HUVEC	blood vessel:	n/a
20	chr1:76080294-76080344	BJ	skin:	n/a
21	chr1:76080294-76080344	HepG2	liver:	n/a
22	chr1:76080924-76080974	HL-60	blood:	n/a
23	chr1:76080727-76080777	HRCEpiC	kidney:	n/a
24	chr1:76082066-76082116	SKMC	muscle:	n/a
25	chr1:76080410-76080460	AG10803	skin:	n/a
26	chr1:76081408-76081458	CMK	blood:	n/a
27	chr1:76080924-76080974	SAEC	small airway:	n/a
28	chr1:76079177-76079227	CMK	blood:	n/a
29	chr1:76085151-76085201	U87	brain:	n/a
30	chr1:76080924-76080974	AoSMC	blood vessel:	n/a
31	chr1:76081379-76081429	GM12878	blood:	n/a
32	chr1:76082568-76082618	HRCEpiC	kidney:	n/a
33	chr1:76079833-76079883	ProgFib	skin:	n/a
34	chr1:76082568-76082618	AG09309	skin:	n/a
35	chr1:76077832-76077882	NHDF-neo	bronchial:	n/a
36	chr1:76085151-76085201	HEEpiC	esophagus:	n/a
37	chr1:76081379-76081429	GM12891	blood:	n/a
38	chr1:76078230-76078280	T-47D	breast:	n/a
39	chr1:76080727-76080777	PFSK-1	brain:	n/a
40	chr1:76082173-76082223	LNCaP	prostate:	n/a
41	chr1:76077832-76077882	HCF	heart:	n/a
42	chr1:76080684-76080734	Jurkat	blood:	n/a
43	chr1:76053565-76053615	AG04449	skin:	fetal
44	chr1:76082173-76082223	Jurkat	blood:	n/a
45	chr1:76079177-76079227	NHDF-neo	bronchial:	n/a
46	chr1:76085151-76085201	NT2-D1	testis:	n/a
47	chr1:76081962-76082012	AG10803	skin:	n/a
48	chr1:76081272-76081322	IMR90	lung:	fetal
49	chr1:76080294-76080344	PANC-1	pancreas:	n/a
50	chr1:76081272-76081322	NT2-D1	testis:	n/a

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:76081387..76081887-chr15:39080643..39081147,2	Hela-S3	cervix:
2	chr1:75985522..75987220-chr1:75991522..75993115,2	K562	blood:
3	chr1:76080604..76083289-chr1:76094142..76096069,2	K562	blood:
4	chr1:76116317..76118957-chr1:76120302..76123457,3	K562	blood:
5	chr1:76073216..76076150-chr1:76081319..76083961,2	MCF-7	breast:
6	chr1:76102793..76106233-chr1:76108594..76111145,3	K562	blood:
7	chr1:76098237..76098781-chr1:76108716..76109281,2	K562	blood:
8	chr1:76026343..76028341-chr1:76031572..76034136,2	K562	blood:
9	chr1:76071710..76074403-chr1:76079679..76081378,2	K562	blood:
10	chr1:76103722..76106233-chr1:76108885..76111145,2	K562	blood:
11	chr1:75933652..75935311-chr1:76250222..76252176,2	K562	blood:
12	chr1:76097324..76099781-chr1:76183811..76186655,2	K562	blood:
13	chr1:76020704..76023494-chr1:76034910..76036939,2	K562	blood:
14	chr1:76094932..76097642-chr1:76105459..76107452,2	K562	blood:
15	chr1:76071710..76074403-chr1:76079679..76081378,2	K562	blood:
16	chr1:76049895..76051572-chr1:76068803..76071353,2	K562	blood:
17	chr1:76020704..76023494-chr1:76034910..76036939,2	K562	blood:
18	chr1:76049895..76051572-chr1:76068803..76071353,2	K562	blood:
19	chr1:76079907..76082887-chr11:62607623..62609125,2	K562	blood:
20	chr1:76064706..76067511-chr1:76072450..76074334,2	K562	blood:
21	chr1:76027597..76030890-chr1:76036483..76038711,3	K562	blood:
22	chr1:75993617..75995152-chr1:75995509..75998505,2	K562	blood:
23	chr1:76083373..76085148-chr1:76086743..76089714,2	MCF-7	breast:
24	chr1:75939435..75941106-chr1:75956675..75959314,2	K562	blood:
25	chr1:76066835..76069254-chr1:76079406..76081859,2	MCF-7	breast:
26	chr1:76048770..76050841-chr1:76082825..76084870,2	MCF-7	breast:
27	chr1:75939435..75941106-chr1:75956675..75959314,2	K562	blood:
28	chr1:75913816..75916653-chr1:75939102..75941877,2	K562	blood:
29	chr1:76070009..76076148-chr1:76078248..76081967,7	K562	blood:
30	chr1:76081387..76082907-chr17:41398843..41401870,3	K562	blood:
31	chr1:75887927..75890320-chr1:76006872..76008474,2	K562	blood:
32	chr1:75964383..75965944-chr1:75967209..75969996,2	K562	blood:
33	chr1:75984267..75985784-chr1:76081741..76084002,2	K562	blood:
34	chr1:75731173..75731698-chr1:76097693..76098339,2	MCF-7	breast:
35	chr1:76048770..76050841-chr1:76082825..76084870,2	MCF-7	breast:
36	chr1:75984267..75985784-chr1:76081741..76084002,2	K562	blood:
37	chr1:76081802..76083861-chr1:76085137..76086923,2	K562	blood:
38	chr1:76094259..76097858-chr1:76188776..76191867,4	K562	blood:
39	chr1:76066835..76069254-chr1:76079406..76081859,2	MCF-7	breast:
40	chr1:76087110..76089218-chr1:76095459..76097902,2	MCF-7	breast:
41	chr1:76098237..76098781-chr1:76108716..76109281,2	K562	blood:
42	chr1:75959031..75961089-chr1:75965586..75967160,2	MCF-7	breast:
43	chr1:76096029..76098574-chr1:76101114..76103972,2	K562	blood:
44	chr1:76080604..76083289-chr1:76094142..76096069,2	K562	blood:
45	chr1:75934636..75936669-chr1:76193127..76195034,2	K562	blood:
46	chr1:76080033..76082466-chr1:76250224..76251859,2	MCF-7	breast:
47	chr1:76031520..76033878-chr1:76036430..76038361,2	K562	blood:
48	chr1:76027597..76030890-chr1:76036483..76038711,3	K562	blood:
49	chr1:76064706..76067511-chr1:76072450..76074334,2	K562	blood:
50	chr1:76083373..76085148-chr1:76086743..76089714,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC44A5-4	chr1:76105925-76108177	NONHSAT003984
2	lnc-ACADM-2	chr1:75987247-75987916	NONHSAT003981
3	lnc-SLC44A5-4	chr1:76107988-76108177	NONHSAT003985
4	lnc-SLC44A5-4	chr1:76103852-76104725	NONHSAT003984

No data

Variant related genes	Relation type
SLC44A5	TF binding region
ENSG00000230863	TF binding region
ENSG00000213579	TF binding region
RNU6-503P	TF binding region
ENSG00000224493	TF binding region
SLC44A5	CpG island
ENSG00000230863	CpG island
ENSG00000213579	CpG island
RNU6-503P	CpG island
ENSG00000224493	CpG island
ENSG00000057468	chromatin interactions
ENSG00000178193	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000137955	chromatin interactions
ENSG00000117054	chromatin interactions
ENSG00000224493	chromatin interactions

Extended variants
information (count: 3768 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:3768 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149027221	chr1:75933694-75933695	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs112822263	chr1:75933722-75933723	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs186025414	chr1:75933741-75933742	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs552826113	chr1:75933787-75933788	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs191175695	chr1:75933969-75933970	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs538212382	chr1:75933988-75933989	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs144930033	chr1:75934070-75934071	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs376831522	chr1:75934072-75934073	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs575251441	chr1:75934098-75934099	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs182497127	chr1:75934138-75934139	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs542380387	chr1:75934191-75934192	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs573339462	chr1:75934192-75934193	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs138753170	chr1:75934202-75934203	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs565546083	chr1:75934225-75934226	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs532563925	chr1:75934258-75934259	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs76720110	chr1:75934267-75934268	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs544573238	chr1:75934290-75934291	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs76110160	chr1:75934301-75934302	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs75677955	chr1:75934306-75934307	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs75627603	chr1:75934324-75934325	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs530604263	chr1:75934325-75934326	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs530255232	chr1:75934346-75934347	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs141755249	chr1:75934400-75934401	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs528080584	chr1:75934441-75934442	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs561166294	chr1:75934534-75934535	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs528243398	chr1:75934536-75934537	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs546504828	chr1:75934576-75934577	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs571167617	chr1:75934632-75934633	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs538247193	chr1:75934638-75934639	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs188080658	chr1:75934639-75934640	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs568749102	chr1:75934695-75934696	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs536378378	chr1:75934752-75934753	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs554342825	chr1:75934784-75934785	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs573494608	chr1:75934852-75934853	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs192490493	chr1:75934869-75934870	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs559298316	chr1:75934882-75934883	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs551438879	chr1:75934891-75934892	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs571565220	chr1:75935012-75935013	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs183072012	chr1:75935045-75935046	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs574721973	chr1:75935065-75935066	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs537588921	chr1:75935083-75935084	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs542329064	chr1:75935124-75935125	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs560348412	chr1:75935129-75935130	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs372327014	chr1:75935143-75935144	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs200442047	chr1:75935147-75935148	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs201264258	chr1:75935148-75935149	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs199596796	chr1:75935149-75935150	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs74898896	chr1:75935158-75935159	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs546341468	chr1:75935165-75935166	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs200702981	chr1:75935170-75935171	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:758 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:75934800-75935000	Enhancers	K562	blood
2	chr1:75935000-75935400	Flanking Active TSS	K562	blood
3	chr1:75935400-75935800	Enhancers	K562	blood
4	chr1:75935800-75936800	Flanking Active TSS	K562	blood
5	chr1:75936000-75937200	Enhancers	Fetal Heart	heart
6	chr1:75936800-75937200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr1:75936800-75937800	Enhancers	K562	blood
8	chr1:75937800-75938200	Flanking Active TSS	K562	blood
9	chr1:75938000-75941000	Enhancers	HUVEC	blood vessel
10	chr1:75938200-75938400	Enhancers	K562	blood
11	chr1:75938200-75939000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr1:75938400-75939200	Flanking Active TSS	K562	blood
13	chr1:75939200-75939400	Enhancers	K562	blood
14	chr1:75939400-75941000	Weak transcription	K562	blood
15	chr1:75941000-75941800	Enhancers	K562	blood
16	chr1:75948200-75949200	Enhancers	HUVEC	blood vessel
17	chr1:75950200-75950600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr1:75950200-75950600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr1:75953000-75953600	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr1:75953200-75953600	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr1:75956800-75958000	Enhancers	HUVEC	blood vessel
22	chr1:75957600-75958600	Enhancers	HepG2	liver
23	chr1:75958400-75959000	Enhancers	Fetal Intestine Large	intestine
24	chr1:75965200-75965400	Enhancers	Fetal Brain Female	brain
25	chr1:75965600-75966800	Weak transcription	Fetal Brain Female	brain
26	chr1:75966400-75969400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr1:75966800-75967400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr1:75966800-75968800	Enhancers	Brain Germinal Matrix	brain
29	chr1:75966800-75969000	Enhancers	Fetal Brain Female	brain
30	chr1:75967000-75969600	Enhancers	Fetal Brain Male	brain
31	chr1:75967200-75968000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr1:75967200-75969600	Enhancers	K562	blood
33	chr1:75967400-75967800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr1:75967800-75968000	Enhancers	Fetal Heart	heart
35	chr1:75968400-75969200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr1:75968400-75969600	Enhancers	HUVEC	blood vessel
37	chr1:75968600-75968800	Enhancers	Fetal Heart	heart
38	chr1:75981200-75981600	Enhancers	Fetal Heart	heart
39	chr1:75982600-75983200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr1:75982800-75983000	Enhancers	Fetal Brain Female	brain
41	chr1:75982800-75983200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr1:75982800-75983400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr1:75982800-75983800	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr1:75982800-75984600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr1:75982800-75984600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr1:75982800-75985400	Weak transcription	K562	blood
47	chr1:75983000-75984400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr1:75983000-75985800	Weak transcription	Fetal Brain Female	brain
49	chr1:75983200-75983600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr1:75983200-75985400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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