Variant report

Variant	esv2756846
Chromosome Location	chr1:76083408-76156986
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:583)
CpG islands
(count:183)
Chromatin interactive
region (count:45)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:583 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:76156263-76156463	K562	blood:	n/a	n/a
2	ARID3A	chr1:76142701-76143423	K562	blood:	n/a	n/a
3	ARID3A	chr1:76105897-76106242	K562	blood:	n/a	n/a
4	ARID3A	chr1:76143217-76143395	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:76127609-76127665	K562	blood:	n/a	n/a
6	ARID3A	chr1:76138415-76138772	K562	blood:	n/a	n/a
7	ATF1	chr1:76109354-76109542	K562	blood:	n/a	n/a
8	ATF1	chr1:76139698-76139874	K562	blood:	n/a	n/a
9	ATF1	chr1:76156227-76156551	K562	blood:	n/a	n/a
10	ATF1	chr1:76105885-76106222	K562	blood:	n/a	n/a
11	ATF2	chr1:76095599-76095993	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr1:76138498-76138845	K562	blood:	n/a	n/a
13	BACH1	chr1:76138455-76138930	K562	blood:	n/a	n/a
14	BACH1	chr1:76137820-76137966	K562	blood:	n/a	n/a
15	BACH1	chr1:76137871-76139155	H1-hESC	embryonic stem cell:	n/a	n/a
16	BHLHE40	chr1:76107180-76107438	K562	blood:	n/a	n/a
17	BHLHE40	chr1:76098240-76098424	GM12878	blood:	n/a	n/a
18	BHLHE40	chr1:76137936-76138902	K562	blood:	n/a	n/a
19	BHLHE40	chr1:76105917-76106244	K562	blood:	n/a	n/a
20	BHLHE40	chr1:76105293-76105429	K562	blood:	n/a	n/a
21	BRCA1	chr1:76138437-76138629	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr1:76138277-76138932	K562	blood:	n/a	n/a
23	CBX3	chr1:76112759-76113226	K562	blood:	n/a	n/a
24	CCNT2	chr1:76156253-76156492	K562	blood:	n/a	n/a
25	CCNT2	chr1:76105959-76106219	K562	blood:	n/a	n/a
26	CEBPB	chr1:76097115-76097389	K562	blood:	n/a	chr1:76097287-76097298
27	CEBPB	chr1:76105433-76105469	K562	blood:	n/a	n/a
28	CEBPB	chr1:76123595-76123716	A549	lung:	n/a	chr1:76123673-76123684
29	CEBPB	chr1:76123509-76123812	HepG2	liver:	n/a	chr1:76123673-76123684
30	CEBPB	chr1:76097115-76097483	HepG2	liver:	n/a	chr1:76097287-76097298
31	CEBPB	chr1:76107117-76107372	K562	blood:	n/a	n/a
32	CEBPB	chr1:76103067-76103358	K562	blood:	n/a	n/a
33	CEBPB	chr1:76097153-76097386	MCF-7	breast:	n/a	chr1:76097287-76097298
34	CEBPB	chr1:76151060-76151260	HepG2	liver:	n/a	chr1:76151076-76151087
35	CEBPB	chr1:76097234-76097355	HepG2	liver:	n/a	chr1:76097287-76097298
36	CEBPB	chr1:76150919-76151183	A549	lung:	n/a	chr1:76151076-76151087
37	CEBPB	chr1:76156353-76156661	K562	blood:	n/a	n/a
38	CEBPB	chr1:76097144-76097360	IMR90	lung:	n/a	chr1:76097287-76097298
39	CEBPB	chr1:76103189-76103319	A549	lung:	n/a	n/a
40	CEBPB	chr1:76084110-76084475	MCF-7	breast:	n/a	n/a
41	CEBPB	chr1:76150911-76151260	K562	blood:	n/a	chr1:76151076-76151087
42	CEBPB	chr1:76151018-76151218	IMR90	lung:	n/a	chr1:76151076-76151087
43	CEBPB	chr1:76084038-76084443	MCF-7	breast:	n/a	n/a
44	CEBPB	chr1:76107129-76107469	K562	blood:	n/a	n/a
45	CHD2	chr1:76139304-76139502	K562	blood:	n/a	n/a
46	CHD2	chr1:76138617-76138632	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr1:76143852-76143884	K562	blood:	n/a	n/a
48	CHD2	chr1:76138594-76138636	HepG2	liver:	n/a	n/a
49	CHD2	chr1:76137806-76138079	HepG2	liver:	n/a	n/a
50	CHD2	chr1:76138563-76138824	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:76138023-76138073	SKMC	muscle:	n/a
2	chr1:76095838-76095888	PrEC	prostate:	n/a
3	chr1:76085151-76085201	AG09309	skin:	n/a
4	chr1:76138023-76138073	T-47D	breast:	n/a
5	chr1:76095838-76095888	NH-A	brain:	n/a
6	chr1:76085151-76085201	CMK	blood:	n/a
7	chr1:76085151-76085201	A549	lung:	n/a
8	chr1:76085151-76085201	GM19239	blood:	n/a
9	chr1:76138023-76138073	NHDF-neo	bronchial:	n/a
10	chr1:76095838-76095888	AG04450	lung:	fetal
11	chr1:76085151-76085201	HPAEpiC	pulmonary alveolar:	n/a
12	chr1:76138023-76138073	GM12891	blood:	n/a
13	chr1:76138023-76138073	GM12878	blood:	n/a
14	chr1:76138023-76138073	U87	brain:	n/a
15	chr1:76138023-76138073	HRE	kidney:	n/a
16	chr1:76138023-76138073	HCM	heart:	n/a
17	chr1:76095838-76095888	AG09319	gingival:	n/a
18	chr1:76085151-76085201	NH-A	brain:	n/a
19	chr1:76085151-76085201	BE2_C	brain:	n/a
20	chr1:76085151-76085201	HRCEpiC	kidney:	n/a
21	chr1:76138023-76138073	A549	lung:	n/a
22	chr1:76085151-76085201	NB4	blood:	n/a
23	chr1:76085151-76085201	ProgFib	skin:	n/a
24	chr1:76085151-76085201	H1-hESC	embryonic stem cell:	embryo
25	chr1:76138023-76138073	ProgFib	skin:	n/a
26	chr1:76085151-76085201	HNPCEpiC	eye:	n/a
27	chr1:76095838-76095888	HCPEpiC	choroid plexus:	n/a
28	chr1:76138023-76138073	NB4	blood:	n/a
29	chr1:76095838-76095888	HRCEpiC	kidney:	n/a
30	chr1:76138023-76138073	NH-A	brain:	n/a
31	chr1:76085151-76085201	RPTEC	kidney:	n/a
32	chr1:76138023-76138073	PFSK-1	brain:	n/a
33	chr1:76095838-76095888	BJ	skin:	n/a
34	chr1:76085151-76085201	HL-60	blood:	n/a
35	chr1:76085151-76085201	AG10803	skin:	n/a
36	chr1:76138023-76138073	GM12892	blood:	n/a
37	chr1:76095838-76095888	U87	brain:	n/a
38	chr1:76095838-76095888	LNCaP	prostate:	n/a
39	chr1:76085151-76085201	SAEC	small airway:	n/a
40	chr1:76095838-76095888	SK-N-SH_RA	brain:	n/a
41	chr1:76138023-76138073	SK-N-SH	brain:	n/a
42	chr1:76138023-76138073	HMEC	breast:	n/a
43	chr1:76138023-76138073	AoSMC	blood vessel:	n/a
44	chr1:76095838-76095888	HCM	heart:	n/a
45	chr1:76085151-76085201	HCM	heart:	n/a
46	chr1:76138023-76138073	MCF-7	breast:	n/a
47	chr1:76138023-76138073	HAEpiC	amniotic membrane:	n/a
48	chr1:76138023-76138073	Caco-2	colon:	n/a
49	chr1:76095838-76095888	MCF-7	breast:	n/a
50	chr1:76085151-76085201	AG04449	skin:	fetal

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:76103722..76106233-chr1:76108885..76111145,2	K562	blood:
2	chr1:76096029..76098574-chr1:76101114..76103972,2	K562	blood:
3	chr1:76073216..76076150-chr1:76081319..76083961,2	MCF-7	breast:
4	chr1:76103722..76106233-chr1:76108885..76111145,2	K562	blood:
5	chr1:76140961..76144068-chr1:76250261..76252961,3	K562	blood:
6	chr1:75731173..75731698-chr1:76097693..76098339,2	MCF-7	breast:
7	chr1:76116317..76118957-chr1:76120302..76123457,3	K562	blood:
8	chr1:76094932..76097642-chr1:76105459..76107452,2	K562	blood:
9	chr1:76153507..76155716-chr1:76158535..76161147,2	K562	blood:
10	chr1:76088182..76090967-chr1:76093940..76095559,2	K562	blood:
11	chr1:76154691..76156608-chr1:76251098..76253830,2	K562	blood:
12	chr1:76156186..76158840-chr1:76189632..76191650,2	K562	blood:
13	chr1:76138876..76140835-chr1:76251753..76254513,3	K562	blood:
14	chr1:76098237..76098781-chr1:76108716..76109281,2	K562	blood:
15	chr1:76083373..76085148-chr1:76086743..76089714,2	MCF-7	breast:
16	chr1:76105051..76106564-chr1:76262176..76264540,2	K562	blood:
17	chr1:76097324..76099781-chr1:76183811..76186655,2	K562	blood:
18	chr1:76094932..76097642-chr1:76105459..76107452,2	K562	blood:
19	chr1:76138718..76140997-chr1:76142345..76144918,2	K562	blood:
20	chr1:76140670..76143009-chr1:76255806..76258053,2	K562	blood:
21	chr1:76079931..76081989-chr1:76083963..76086787,2	K562	blood:
22	chr1:76152720..76155791-chr1:76253617..76257786,3	K562	blood:
23	chr1:76102793..76106233-chr1:76108594..76111145,3	K562	blood:
24	chr1:76135960..76138598-chr1:76257398..76259099,2	K562	blood:
25	chr1:76136512..76138761-chr1:76260290..76263855,4	K562	blood:
26	chr1:76087110..76089218-chr1:76095459..76097902,2	MCF-7	breast:
27	chr1:76138718..76140997-chr1:76142345..76144918,2	K562	blood:
28	chr1:76116317..76118957-chr1:76120302..76123457,3	K562	blood:
29	chr1:76096029..76098574-chr1:76101114..76103972,2	K562	blood:
30	chr1:76135232..76136937-chr1:76193196..76195615,2	K562	blood:
31	chr1:76141089..76142781-chr1:76250261..76252071,2	K562	blood:
32	chr1:76102793..76106233-chr1:76108594..76111145,3	K562	blood:
33	chr1:76098237..76098781-chr1:76108716..76109281,2	K562	blood:
34	chr1:76139328..76142229-chr1:76158809..76161190,2	K562	blood:
35	chr1:76048770..76050841-chr1:76082825..76084870,2	MCF-7	breast:
36	chr1:76094259..76097858-chr1:76188776..76191867,4	K562	blood:
37	chr1:76083373..76085148-chr1:76086743..76089714,2	MCF-7	breast:
38	chr1:75698929..75699675-chr1:76097798..76098711,3	K562	blood:
39	chr1:76087110..76089218-chr1:76095459..76097902,2	MCF-7	breast:
40	chr1:76081802..76083861-chr1:76085137..76086923,2	K562	blood:
41	chr1:76088182..76090967-chr1:76093940..76095559,2	K562	blood:
42	chr1:76081802..76083861-chr1:76085137..76086923,2	K562	blood:
43	chr1:76136446..76138259-chr1:76189741..76191373,2	K562	blood:
44	chr1:76080604..76083289-chr1:76094142..76096069,2	K562	blood:
45	chr1:75984267..75985784-chr1:76081741..76084002,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC44A5-4	chr1:76143415-76143463	NONHSAT003985
2	lnc-SLC44A5-4	chr1:76107988-76108177	NONHSAT003985
3	lnc-SLC44A5-4	chr1:76103852-76104725	NONHSAT003984
4	lnc-SLC44A5-4	chr1:76105925-76108177	NONHSAT003984

No data

Variant related genes	Relation type
ENSG00000230863	TF binding region
ENSG00000230863	CpG island
ENSG00000057468	chromatin interactions
ENSG00000207241	chromatin interactions
ENSG00000178193	chromatin interactions
ENSG00000201487	chromatin interactions
ENSG00000137955	chromatin interactions
ENSG00000117054	chromatin interactions
ENSG00000206620	chromatin interactions

Extended variants
information (count: 1363 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:1363 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2057519	chr1:76083408-76083409	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs183191955	chr1:76083411-76083412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187716142	chr1:76083420-76083421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs529697502	chr1:76083435-76083436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541771681	chr1:76083495-76083496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143165246	chr1:76083647-76083648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs4949869	chr1:76083667-76083668	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs146640680	chr1:76083681-76083682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs552371971	chr1:76083696-76083697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs192690807	chr1:76083702-76083703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185747069	chr1:76083703-76083704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147176759	chr1:76083733-76083734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs550100460	chr1:76083735-76083736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576403783	chr1:76083752-76083753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs34490785	chr1:76083825-76083826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535483560	chr1:76083847-76083848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190452171	chr1:76083860-76083861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560274959	chr1:76083919-76083920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545468631	chr1:76083927-76083928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539958078	chr1:76083936-76083937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558262224	chr1:76083958-76083959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs141465313	chr1:76083976-76083977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538030708	chr1:76084042-76084043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs34200256	chr1:76084057-76084058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556508252	chr1:76084061-76084062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574630605	chr1:76084062-76084063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541485337	chr1:76084063-76084064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192129857	chr1:76084068-76084069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143880871	chr1:76084119-76084120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200701128	chr1:76084187-76084188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545537520	chr1:76084206-76084207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11585962	chr1:76084207-76084208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146859273	chr1:76084218-76084219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs55923428	chr1:76084231-76084232	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs35811748	chr1:76084269-76084270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148970015	chr1:76084334-76084335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562264219	chr1:76084399-76084400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529557253	chr1:76084421-76084422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143079364	chr1:76084431-76084432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184214776	chr1:76084448-76084449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113733419	chr1:76084451-76084452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561612990	chr1:76084478-76084479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552475789	chr1:76084540-76084541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534507831	chr1:76084556-76084557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550472752	chr1:76084566-76084567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551946118	chr1:76084585-76084586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570124361	chr1:76084589-76084590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538043274	chr1:76084662-76084663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188631994	chr1:76084697-76084698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556296762	chr1:76084704-76084705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:140 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76082600-76085200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:76083200-76084000	Enhancers	Fetal Brain Female	brain
3	chr1:76091200-76092200	Enhancers	Dnd41	blood
4	chr1:76091800-76092800	Enhancers	HUVEC	blood vessel
5	chr1:76092400-76095800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:76094400-76094800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
7	chr1:76094600-76094800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
8	chr1:76094600-76095000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr1:76094600-76095400	Enhancers	HepG2	liver
10	chr1:76094600-76096200	Enhancers	H1 Cell Line	embryonic stem cell
11	chr1:76094600-76096800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr1:76094800-76096200	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr1:76094800-76096200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr1:76094800-76096800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr1:76095000-76095200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:76095000-76095200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:76095000-76096200	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr1:76095000-76096600	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr1:76095200-76095400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr1:76095200-76096200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:76095200-76096200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr1:76095200-76096200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr1:76095200-76096200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr1:76095400-76095600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr1:76095400-76096200	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr1:76095400-76096600	Weak transcription	HepG2	liver
27	chr1:76095400-76096800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr1:76095600-76096200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:76095800-76096200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr1:76095800-76096200	Enhancers	H9 Cell Line	embryonic stem cell
31	chr1:76095800-76096200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr1:76095800-76096200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr1:76096200-76098600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr1:76096400-76097600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr1:76096600-76097200	Enhancers	HepG2	liver
36	chr1:76098600-76098800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr1:76104400-76104800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr1:76104800-76105200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr1:76105200-76106200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr1:76105200-76106200	Enhancers	Pancreas	Pancrea
41	chr1:76105200-76106400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr1:76105200-76106400	Enhancers	K562	blood
43	chr1:76105200-76106600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr1:76105800-76106200	Enhancers	Esophagus	oesophagus
45	chr1:76108000-76108200	Enhancers	Esophagus	oesophagus
46	chr1:76109200-76109800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr1:76121000-76121400	ZNF genes & repeats	Aorta	Aorta
48	chr1:76128400-76129400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr1:76128800-76129200	Enhancers	HepG2	liver
50	chr1:76129200-76136400	Weak transcription	HepG2	liver

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