Variant report

Variant	nsv874345
Chromosome Location	chr2:77912770-78199268
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:78166529-78166714	K562	blood:	n/a	n/a
2	BACH1	chr2:78043808-78043996	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:78056821-78057163	H1-hESC	embryonic stem cell:	n/a	n/a
4	BDP1	chr2:78181978-78182355	K562	blood:	n/a	n/a
5	BHLHE40	chr2:78189217-78189406	HepG2	liver:	n/a	n/a
6	CBX3	chr2:78182148-78182464	K562	blood:	n/a	n/a
7	CBX3	chr2:78182081-78182419	K562	blood:	n/a	n/a
8	CCNT2	chr2:78110616-78110816	K562	blood:	n/a	n/a
9	CEBPB	chr2:78175119-78175452	HepG2	liver:	n/a	chr2:78175273-78175284 chr2:78175274-78175283 chr2:78175272-78175285 chr2:78175272-78175285 chr2:78175271-78175288 chr2:78175272-78175283
10	CEBPB	chr2:78186368-78186396	K562	blood:	n/a	n/a
11	CEBPB	chr2:78167660-78167813	H1-hESC	embryonic stem cell:	n/a	chr2:78167759-78167770
12	CEBPB	chr2:78177783-78177983	A549	lung:	n/a	n/a
13	CEBPB	chr2:77995692-77996037	HepG2	liver:	n/a	chr2:77995852-77995863
14	CEBPB	chr2:78167589-78167947	HepG2	liver:	n/a	chr2:78167759-78167770
15	CEBPB	chr2:78162903-78163211	K562	blood:	n/a	chr2:78163175-78163186 chr2:78163032-78163043
16	CEBPB	chr2:78167635-78167910	A549	lung:	n/a	chr2:78167759-78167770
17	CEBPB	chr2:78079324-78079534	A549	lung:	n/a	chr2:78079391-78079404 chr2:78079423-78079434 chr2:78079391-78079402
18	CEBPB	chr2:78165625-78165964	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:78175125-78175447	A549	lung:	n/a	chr2:78175273-78175284 chr2:78175274-78175283 chr2:78175272-78175285 chr2:78175272-78175285 chr2:78175271-78175288 chr2:78175272-78175283
20	CEBPB	chr2:78175125-78175449	IMR90	lung:	n/a	chr2:78175273-78175284 chr2:78175274-78175283 chr2:78175272-78175285 chr2:78175272-78175285 chr2:78175271-78175288 chr2:78175272-78175283
21	CEBPB	chr2:78112510-78112626	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:77995750-77995921	HepG2	liver:	n/a	chr2:77995852-77995863
23	CEBPB	chr2:78018338-78018524	HepG2	liver:	n/a	chr2:78018470-78018483 chr2:78018453-78018464
24	CEBPB	chr2:78099017-78099072	A549	lung:	n/a	n/a
25	CEBPB	chr2:78162870-78163199	HepG2	liver:	n/a	chr2:78163175-78163186 chr2:78163032-78163043
26	CEBPB	chr2:78152262-78152552	HepG2	liver:	n/a	chr2:78152391-78152402
27	CEBPB	chr2:78162989-78163068	H1-hESC	embryonic stem cell:	n/a	chr2:78163032-78163043
28	CEBPB	chr2:78167632-78167925	IMR90	lung:	n/a	chr2:78167759-78167770
29	CEBPB	chr2:78092232-78092239	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr2:78167724-78167821	K562	blood:	n/a	chr2:78167759-78167770
31	CEBPB	chr2:78079267-78079555	HepG2	liver:	n/a	chr2:78079391-78079404 chr2:78079423-78079434 chr2:78079391-78079402
32	CEBPB	chr2:78162868-78163163	A549	lung:	n/a	chr2:78163032-78163043
33	CEBPB	chr2:78029044-78029185	HepG2	liver:	n/a	chr2:78029126-78029139 chr2:78029127-78029138
34	CEBPB	chr2:77950062-77950237	HepG2	liver:	n/a	chr2:77950092-77950103
35	CEBPB	chr2:77946096-77946340	A549	lung:	n/a	chr2:77946226-77946239 chr2:77946226-77946237 chr2:77946226-77946239
36	CEBPB	chr2:77955576-77955730	HepG2	liver:	n/a	chr2:77955582-77955593
37	CEBPB	chr2:77946087-77946386	HepG2	liver:	n/a	chr2:77946226-77946239 chr2:77946226-77946237 chr2:77946226-77946239
38	CEBPB	chr2:78079311-78079511	IMR90	lung:	n/a	chr2:78079391-78079404 chr2:78079423-78079434 chr2:78079391-78079402
39	CHD2	chr2:77981206-77981340	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr2:78033617-78033669	Lung_OC	lung:	n/a	n/a
41	CTCF	chr2:78182120-78182270	AG09309	skin:	n/a	chr2:78182125-78182138
42	CTCF	chr2:78098067-78098103	GM10248	blood:	n/a	n/a
43	CTCF	chr2:78182240-78182390	SK-N-SH_RA	brain:	n/a	chr2:78182274-78182283 chr2:78182269-78182285 chr2:78182263-78182284 chr2:78182271-78182281 chr2:78182270-78182283 chr2:78182268-78182286
44	CTCF	chr2:78182192-78182310	GM12892	blood:	n/a	chr2:78182274-78182283 chr2:78182269-78182285 chr2:78182263-78182284 chr2:78182271-78182281 chr2:78182270-78182283 chr2:78182268-78182286
45	CTCF	chr2:78182100-78182250	HRE	kidney:	n/a	chr2:78182125-78182138
46	CTCF	chr2:78182200-78182350	HCFaa	heart:	n/a	chr2:78182274-78182283 chr2:78182269-78182285 chr2:78182263-78182284 chr2:78182271-78182281 chr2:78182270-78182283 chr2:78182268-78182286
47	CTCF	chr2:77916558-77916601	Medullo	brain:	n/a	n/a
48	CTCF	chr2:78182215-78182328	GM19239	blood:	n/a	chr2:78182274-78182283 chr2:78182269-78182285 chr2:78182263-78182284 chr2:78182271-78182281 chr2:78182270-78182283 chr2:78182268-78182286
49	CTCF	chr2:78182170-78182396	A549	lung:	n/a	chr2:78182274-78182283 chr2:78182269-78182285 chr2:78182263-78182284 chr2:78182271-78182281 chr2:78182270-78182283 chr2:78182268-78182286
50	CTCF	chr2:78182220-78182370	GM12873	blood:	n/a	chr2:78182274-78182283 chr2:78182269-78182285 chr2:78182263-78182284 chr2:78182271-78182281 chr2:78182270-78182283 chr2:78182268-78182286

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:77961984-77962034	ProgFib	skin:	n/a
2	chr2:77961984-77962034	ProgFib	skin:	n/a
3	chr2:78182350-78182400	NH-A	brain:	n/a
4	chr2:77981162-77981212	HPAEpiC	pulmonary alveolar:	n/a
5	chr2:78182187-78182237	Caco-2	colon:	n/a
6	chr2:78182187-78182237	CMK	blood:	n/a
7	chr2:77981162-77981212	SAEC	small airway:	n/a
8	chr2:77962212-77962262	RPTEC	kidney:	n/a
9	chr2:78182350-78182400	HNPCEpiC	eye:	n/a
10	chr2:78182350-78182400	NHBE	bronchial:	n/a
11	chr2:77981162-77981212	IMR90	lung:	fetal
12	chr2:77981162-77981212	HCM	heart:	n/a
13	chr2:78182197-78182247	HRE	kidney:	n/a
14	chr2:77962212-77962262	SAEC	small airway:	n/a
15	chr2:78182197-78182247	U87	brain:	n/a
16	chr2:78182350-78182400	BE2_C	brain:	n/a
17	chr2:77981162-77981212	NHDF-neo	bronchial:	n/a
18	chr2:78182197-78182247	AG04449	skin:	fetal
19	chr2:77962212-77962262	HRCEpiC	kidney:	n/a
20	chr2:78182197-78182247	PrEC	prostate:	n/a
21	chr2:77981162-77981212	RPTEC	kidney:	n/a
22	chr2:78182197-78182247	K562	blood:	n/a
23	chr2:77961984-77962034	SAEC	small airway:	n/a
24	chr2:77962212-77962262	AoSMC	blood vessel:	n/a
25	chr2:78182187-78182237	HEEpiC	esophagus:	n/a
26	chr2:77962212-77962262	AG04449	skin:	fetal
27	chr2:78182187-78182237	GM12892	blood:	n/a
28	chr2:78182187-78182237	HCPEpiC	choroid plexus:	n/a
29	chr2:78182350-78182400	GM06990	blood:	n/a
30	chr2:78182187-78182237	GM12878	blood:	n/a
31	chr2:77981162-77981212	BJ	skin:	n/a
32	chr2:77962212-77962262	HRPEpiC	eye:	n/a
33	chr2:78182187-78182237	Hepatocyte	liver:	n/a
34	chr2:78182350-78182400	AG10803	skin:	n/a
35	chr2:78182350-78182400	HRE	kidney:	n/a
36	chr2:77961984-77962034	NH-A	brain:	n/a
37	chr2:78182350-78182400	Jurkat	blood:	n/a
38	chr2:78182197-78182247	IMR90	lung:	fetal
39	chr2:77961984-77962034	U87	brain:	n/a
40	chr2:78182187-78182237	T-47D	breast:	n/a
41	chr2:78182197-78182247	HMEC	breast:	n/a
42	chr2:77961984-77962034	SKMC	muscle:	n/a
43	chr2:77981162-77981212	BE2_C	brain:	n/a
44	chr2:78182197-78182247	ProgFib	skin:	n/a
45	chr2:77962212-77962262	HCM	heart:	n/a
46	chr2:77961984-77962034	HCT-116	colon:	n/a
47	chr2:78182350-78182400	NHDF-neo	bronchial:	n/a
48	chr2:78182350-78182400	SK-N-SH_RA	brain:	n/a
49	chr2:78182350-78182400	H1-hESC	embryonic stem cell:	embryo
50	chr2:77981162-77981212	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:56735169..56737848-chr2:78047828..78049670,2	MCF-7	breast:
2	chr2:77914010..77915510-chr20:60019091..60020639,2	MCF-7	breast:
3	chr1:111007522..111008367-chr2:78191655..78192229,2	MCF-7	breast:
4	chr2:78150104..78151070-chr7:109526792..109527641,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-REG3G-4	chr2:78144828-78145135	NONHSAT071836
2	lnc-LRRTM4-3	chr2:78066895-78067016	NR_110288
3	lnc-REG3G-8	chr2:78187674-78187885	NONHSAT071839
4	lnc-REG3G-8	chr2:78175271-78175410	NONHSAT071839
5	lnc-REG3G-4	chr2:78144362-78144530	NONHSAT071836
6	lnc-REG3G-4	chr2:78144363-78144530	XLOC_001542
7	lnc-REG3G-4	chr2:78143060-78143219	XLOC_001542
8	lnc-REG3G-4	chr2:78144363-78144530	XLOC_001542
9	lnc-REG3G-4	chr2:78143033-78143219	XLOC_001542
10	lnc-LRRTM4-2	chr2:78176532-78176551	XLOC_002173
11	lnc-LRRTM4-3	chr2:78102106-78102188	NR_110288
12	lnc-REG3G-4	chr2:78144829-78145134	NR_110286
13	lnc-REG3G-10	chr2:77996541-77996727	l_1869_chr2:77996540-77998625_testes
14	lnc-REG3G-10	chr2:77997871-77998038	NONHSAT071832
15	lnc-REG3G-10	chr2:77997871-77998038	l_1869_chr2:77996540-77998625_testes
16	lnc-REG3G-9	chr2:78019947-78020151	NONHSAT071834
17	lnc-REG3G-10	chr2:77998337-77998625	l_1869_chr2:77996540-77998625_testes
18	lnc-REG3G-10	chr2:77998337-77998643	NONHSAT071832
19	lnc-LRRTM4-8	chr2:78105961-78106058	ucscGeneNc_uc002snu_2
20	lnc-LRRTM4-3	chr2:78102058-78102188	NONHSAT071835
21	lnc-REG3G-4	chr2:78144874-78145117	XLOC_001542
22	lnc-REG3G-4	chr2:78143060-78143219	NR_110286
23	lnc-REG3G-9	chr2:78019858-78020279	NONHSAT071833
24	lnc-REG3G-10	chr2:77996568-77996727	NONHSAT071832
25	lnc-REG3G-8	chr2:78169364-78169425	NONHSAT071839
26	lnc-REG3G-9	chr2:78013230-78013238	NONHSAT071833
27	lnc-REG3G-9	chr2:78015508-78015637	NONHSAT071833
28	lnc-REG3G-8	chr2:78192534-78192764	NONHSAT071839
29	lnc-LRRTM4-8	chr2:78098667-78099271	ucscGeneNc_uc002snu_2
30	lnc-REG3G-9	chr2:78014667-78014729	NONHSAT071833
31	lnc-LRRTM4-3	chr2:77970822-77970948	NR_110288
32	lnc-REG3G-4	chr2:78143032-78143219	NONHSAT071836
33	lnc-REG3G-8	chr2:78174151-78174300	NONHSAT071839
34	lnc-REG3G-4	chr2:78144829-78145135	XLOC_001542
35	lnc-REG3G-4	chr2:78144363-78144530	NR_110286
36	lnc-LRRTM4-2	chr2:78178164-78178621	XLOC_002173

Variant related genes	Relation type
ENSG00000233605	TF binding region
ENSG00000237077	TF binding region
ENSG00000233605	CpG island
ENSG00000237077	CpG island
ENSG00000202077	chromatin interactions
PDCD4	miRNA target sites
CELF2	miRNA target sites

Extended variants
information (count: 5368 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:5368 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10170086	chr2:77918007-77918008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs547642025	chr2:77918033-77918034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs375167218	chr2:77918102-77918103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs72928045	chr2:77918104-77918105	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs187931220	chr2:77918136-77918137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576387936	chr2:77918150-77918151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538701298	chr2:77918171-77918172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558900401	chr2:77918182-77918183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs572481198	chr2:77918249-77918250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs541100018	chr2:77918264-77918265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190892995	chr2:77918314-77918315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs76724132	chr2:77918318-77918319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140794554	chr2:77918328-77918329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563873216	chr2:77918338-77918339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs10185229	chr2:77918355-77918356	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs74858438	chr2:77918393-77918394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564876933	chr2:77918404-77918405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149756072	chr2:77918433-77918434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs371266606	chr2:77918541-77918542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542157062	chr2:77918550-77918551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567478177	chr2:77918589-77918590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562051362	chr2:77918598-77918599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs115208480	chr2:77918644-77918645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs182071576	chr2:77918690-77918691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186705189	chr2:77918712-77918713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371731260	chr2:77918747-77918748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569890441	chr2:77918760-77918761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192606729	chr2:77918762-77918763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558706987	chr2:77918774-77918775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs566031765	chr2:77918809-77918810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs116742977	chr2:77918813-77918814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554599084	chr2:77918880-77918881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs367748667	chr2:77918931-77918932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531059907	chr2:77918945-77918946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543650146	chr2:77918954-77918955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs557515810	chr2:77918956-77918957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs551929995	chr2:77918980-77918981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs4853333	chr2:77919015-77919016	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs72813201	chr2:77919036-77919037	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs564741908	chr2:77919105-77919106	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs184990995	chr2:77919126-77919127	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs145609664	chr2:77919148-77919149	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs561012115	chr2:77919171-77919172	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs529801377	chr2:77919228-77919229	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs546757371	chr2:77919235-77919236	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs537780163	chr2:77919271-77919272	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs34640013	chr2:77919307-77919308	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs556016022	chr2:77919320-77919321	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs12053244	chr2:77919342-77919343	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs78170812	chr2:77919371-77919372	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Mental retardation	17124404	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Breast cancer	16272173	CNVD
Epilepsy	22083797	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:204 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:77918000-77919000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:77918200-77918800	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr2:77918800-77919200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr2:77919000-77919400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr2:77919200-77919800	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr2:77919400-77920000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:77921600-77921800	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr2:77921800-77922600	Enhancers	Fetal Heart	heart
9	chr2:77940200-77941600	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr2:77940400-77940600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr2:77940400-77941000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr2:77940400-77941400	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr2:77940400-77941400	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr2:77940600-77941000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr2:77940600-77941000	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr2:77940800-77941400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr2:77940800-77941400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr2:77941000-77941400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr2:77948600-77949400	Enhancers	HepG2	liver
20	chr2:77954200-77961800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr2:77961800-77962400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr2:77974000-77975200	Enhancers	HepG2	liver
23	chr2:77975000-77975200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr2:77975200-77975600	Weak transcription	HepG2	liver
25	chr2:77975200-77980800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr2:77975600-77976000	Enhancers	HepG2	liver
27	chr2:77977200-77977600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
28	chr2:77979400-77980000	Enhancers	H9 Cell Line	embryonic stem cell
29	chr2:77980000-77980800	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr2:77980400-77980600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr2:77980600-77980800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
32	chr2:77980600-77981400	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr2:77980600-77981400	Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr2:77980600-77981400	Active TSS	iPS-15b Cell Line	embryonic stem cell
35	chr2:77980600-77981400	Active TSS	iPS-18 Cell Line	embryonic stem cell
36	chr2:77980600-77981400	Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr2:77980600-77981600	Active TSS	H1 Cell Line	embryonic stem cell
38	chr2:77980600-77981600	Active TSS	HUES6 Cell Line	embryonic stem cell
39	chr2:77980800-77981200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
40	chr2:77980800-77981400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr2:77980800-77981400	Active TSS	H9 Cell Line	embryonic stem cell
42	chr2:77980800-77981400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr2:77980800-77981400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr2:77980800-77981600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr2:77980800-77981600	Active TSS	HUES64 Cell Line	embryonic stem cell
46	chr2:77980800-77981600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr2:77994400-77994800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr2:77994600-77995000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr2:77994600-77996200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr2:77995000-77995200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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