Variant report

Variant	esv2757810
Chromosome Location	chr2:77855098-78101551
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:418)
CpG islands
(count:244)
Chromatin interactive
region (count:2)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:418 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:77856705-77856971	HepG2	liver:	n/a	n/a
2	BACH1	chr2:78056821-78057163	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:78043808-78043996	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:77858291-77858408	K562	blood:	n/a	n/a
5	CEBPB	chr2:77866132-77866309	A549	lung:	n/a	chr2:77866208-77866219
6	CEBPB	chr2:77870309-77870701	HepG2	liver:	n/a	n/a
7	CEBPB	chr2:78092232-78092239	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr2:78099017-78099072	A549	lung:	n/a	n/a
9	CEBPB	chr2:77870443-77870684	A549	lung:	n/a	n/a
10	CEBPB	chr2:77955576-77955730	HepG2	liver:	n/a	chr2:77955582-77955593
11	CEBPB	chr2:77893984-77894002	A549	lung:	n/a	n/a
12	CEBPB	chr2:77857855-77858007	HepG2	liver:	n/a	n/a
13	CEBPB	chr2:77946087-77946386	HepG2	liver:	n/a	chr2:77946226-77946239 chr2:77946226-77946237 chr2:77946226-77946239
14	CEBPB	chr2:77995750-77995921	HepG2	liver:	n/a	chr2:77995852-77995863
15	CEBPB	chr2:77866168-77866347	HepG2	liver:	n/a	chr2:77866208-77866219
16	CEBPB	chr2:77946096-77946340	A549	lung:	n/a	chr2:77946226-77946239 chr2:77946226-77946237 chr2:77946226-77946239
17	CEBPB	chr2:77861610-77861945	HepG2	liver:	n/a	chr2:77861765-77861776
18	CEBPB	chr2:77855784-77856051	HepG2	liver:	n/a	chr2:77855924-77855935 chr2:77855922-77855939 chr2:77855923-77855936
19	CEBPB	chr2:77861626-77861952	A549	lung:	n/a	chr2:77861765-77861776
20	CEBPB	chr2:78079267-78079555	HepG2	liver:	n/a	chr2:78079391-78079404 chr2:78079423-78079434 chr2:78079391-78079402
21	CEBPB	chr2:78079324-78079534	A549	lung:	n/a	chr2:78079391-78079404 chr2:78079423-78079434 chr2:78079391-78079402
22	CEBPB	chr2:78029044-78029185	HepG2	liver:	n/a	chr2:78029126-78029139 chr2:78029127-78029138
23	CEBPB	chr2:77870422-77870629	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr2:77878013-77878356	HepG2	liver:	n/a	chr2:77878197-77878206 chr2:77878196-77878207
25	CEBPB	chr2:77861644-77861916	IMR90	lung:	n/a	chr2:77861765-77861776
26	CEBPB	chr2:77893819-77894063	HepG2	liver:	n/a	chr2:77893930-77893941
27	CEBPB	chr2:77893764-77894088	HepG2	liver:	n/a	chr2:77893930-77893941
28	CEBPB	chr2:77861689-77861796	H1-hESC	embryonic stem cell:	n/a	chr2:77861765-77861776
29	CEBPB	chr2:77870317-77870489	K562	blood:	n/a	n/a
30	CEBPB	chr2:78018338-78018524	HepG2	liver:	n/a	chr2:78018470-78018483 chr2:78018453-78018464
31	CEBPB	chr2:78079311-78079511	IMR90	lung:	n/a	chr2:78079391-78079404 chr2:78079423-78079434 chr2:78079391-78079402
32	CEBPB	chr2:77950062-77950237	HepG2	liver:	n/a	chr2:77950092-77950103
33	CEBPB	chr2:77995692-77996037	HepG2	liver:	n/a	chr2:77995852-77995863
34	CHD2	chr2:77981206-77981340	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr2:78037650-78037693	GM10248	blood:	n/a	n/a
36	CTCF	chr2:77962880-77963030	HepG2	liver:	n/a	n/a
37	CTCF	chr2:77916558-77916601	Medullo	brain:	n/a	n/a
38	CTCF	chr2:77962900-77963050	Caco-2	colon:	n/a	n/a
39	CTCF	chr2:77962920-77963070	RPTEC	kidney:	n/a	n/a
40	CTCF	chr2:77963643-77963782	LNCaP	prostate:	n/a	chr2:77963682-77963703
41	CTCF	chr2:77910310-77910325	Medullo	brain:	n/a	n/a
42	CTCF	chr2:77894725-77894782	GM10266	blood:	n/a	n/a
43	CTCF	chr2:77906948-77906955	A549	lung:	n/a	n/a
44	CTCF	chr2:77962940-77963090	HepG2	liver:	n/a	n/a
45	CTCF	chr2:78046932-78046967	GM20000	blood:	n/a	n/a
46	CTCF	chr2:77911824-77911827	MCF-7	breast:	n/a	n/a
47	CTCF	chr2:78098067-78098103	GM10248	blood:	n/a	n/a
48	CTCF	chr2:77911786-77911819	MCF-7	breast:	n/a	n/a
49	CTCF	chr2:78033617-78033669	Lung_OC	lung:	n/a	n/a
50	CTCF	chr2:77999629-77999640	GM10248	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:77856944-77856994	HPAEpiC	pulmonary alveolar:	n/a
2	chr2:77961984-77962034	Hela-S3	cervix:	n/a
3	chr2:77856944-77856994	GM12891	blood:	n/a
4	chr2:77962212-77962262	NHDF-neo	bronchial:	n/a
5	chr2:77856944-77856994	MCF-7	breast:	n/a
6	chr2:77962212-77962262	Jurkat	blood:	n/a
7	chr2:77981162-77981212	Hepatocyte	liver:	n/a
8	chr2:77856944-77856994	AoSMC	blood vessel:	n/a
9	chr2:77962212-77962262	HRE	kidney:	n/a
10	chr2:77961984-77962034	AG04449	skin:	fetal
11	chr2:77961984-77962034	AG04450	lung:	fetal
12	chr2:77856944-77856994	Hela-S3	cervix:	n/a
13	chr2:77856944-77856994	GM06990	blood:	n/a
14	chr2:77961984-77962034	NHDF-neo	bronchial:	n/a
15	chr2:77981162-77981212	Hela-S3	cervix:	n/a
16	chr2:77856944-77856994	AG04449	skin:	fetal
17	chr2:77856944-77856994	AG10803	skin:	n/a
18	chr2:77856944-77856994	BJ	skin:	n/a
19	chr2:77962212-77962262	AG04449	skin:	fetal
20	chr2:77962212-77962262	HPAEpiC	pulmonary alveolar:	n/a
21	chr2:77856944-77856994	HCT-116	colon:	n/a
22	chr2:77981162-77981212	IMR90	lung:	fetal
23	chr2:77962212-77962262	HRPEpiC	eye:	n/a
24	chr2:77962212-77962262	AG10803	skin:	n/a
25	chr2:77961984-77962034	T-47D	breast:	n/a
26	chr2:77856944-77856994	AG09319	gingival:	n/a
27	chr2:77856944-77856994	HAEpiC	amniotic membrane:	n/a
28	chr2:77856944-77856994	HL-60	blood:	n/a
29	chr2:77961984-77962034	RPTEC	kidney:	n/a
30	chr2:77981162-77981212	Caco-2	colon:	n/a
31	chr2:77981162-77981212	H1-hESC	embryonic stem cell:	embryo
32	chr2:77981162-77981212	HRCEpiC	kidney:	n/a
33	chr2:77856944-77856994	HRE	kidney:	n/a
34	chr2:77856944-77856994	HNPCEpiC	eye:	n/a
35	chr2:77962212-77962262	MCF10A-Er-Src	breast:	n/a
36	chr2:77961984-77962034	H1-hESC	embryonic stem cell:	embryo
37	chr2:77961984-77962034	HCM	heart:	n/a
38	chr2:77961984-77962034	ProgFib	skin:	n/a
39	chr2:77961984-77962034	PANC-1	pancreas:	n/a
40	chr2:77981162-77981212	GM12878	blood:	n/a
41	chr2:77981162-77981212	NT2-D1	testis:	n/a
42	chr2:77981162-77981212	HUVEC	blood vessel:	n/a
43	chr2:77856944-77856994	SK-N-SH	brain:	n/a
44	chr2:77961984-77962034	SK-N-SH	brain:	n/a
45	chr2:77981162-77981212	CMK	blood:	n/a
46	chr2:77856944-77856994	CMK	blood:	n/a
47	chr2:77961984-77962034	AG09319	gingival:	n/a
48	chr2:77981162-77981212	AG04450	lung:	fetal
49	chr2:77981162-77981212	GM06990	blood:	n/a
50	chr2:77961984-77962034	HRE	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:77914010..77915510-chr20:60019091..60020639,2	MCF-7	breast:
2	chr17:56735169..56737848-chr2:78047828..78049670,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRTM4-8	chr2:78098667-78099271	ucscGeneNc_uc002snu_2
2	lnc-LRRTM4-1	chr2:77879539-77879735	XLOC_002172
3	lnc-REG3G-9	chr2:78015508-78015637	NONHSAT071833
4	lnc-REG3G-9	chr2:78019947-78020151	NONHSAT071834
5	lnc-REG3G-9	chr2:78014667-78014729	NONHSAT071833
6	lnc-REG3G-9	chr2:78013230-78013238	NONHSAT071833
7	lnc-REG3G-5	chr2:77900177-77900918	XLOC_001541
8	lnc-REG3G-10	chr2:77998337-77998625	l_1869_chr2:77996540-77998625_testes
9	lnc-REG3G-10	chr2:77997871-77998038	l_1869_chr2:77996540-77998625_testes
10	lnc-LRRTM4-3	chr2:77970822-77970948	NR_110288
11	lnc-REG3G-10	chr2:77996568-77996727	NONHSAT071832
12	lnc-LRRTM4-3	chr2:78066895-78067016	NR_110288
13	lnc-REG3G-5	chr2:77899341-77899395	XLOC_001541
14	lnc-REG3G-10	chr2:77996541-77996727	l_1869_chr2:77996540-77998625_testes
15	lnc-REG3G-9	chr2:78019858-78020279	NONHSAT071833
16	lnc-REG3G-10	chr2:77997871-77998038	NONHSAT071832
17	lnc-REG3G-10	chr2:77998337-77998643	NONHSAT071832
18	lnc-LRRTM4-1	chr2:77881708-77881794	XLOC_002172

No data

Variant related genes	Relation type
ENSG00000227088	TF binding region
ENSG00000237077	TF binding region
ENSG00000230968	TF binding region
ENSG00000227088	CpG island
ENSG00000237077	CpG island
ENSG00000230968	CpG island
ENSG00000202077	chromatin interactions
PAPD4	miRNA target sites
RAB34	miRNA target sites

Extended variants
information (count: 5019 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:5019 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189229148	chr2:77855119-77855120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs555066090	chr2:77855145-77855146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs59678860	chr2:77855151-77855152	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs544236307	chr2:77855192-77855193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs192306839	chr2:77855214-77855215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533081225	chr2:77855217-77855218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs4580407	chr2:77855237-77855238	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs560328790	chr2:77855299-77855300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs4286309	chr2:77855304-77855305	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs4286310	chr2:77855363-77855364	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs147745203	chr2:77855387-77855388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183470193	chr2:77855446-77855447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551385521	chr2:77855473-77855474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571388387	chr2:77855518-77855519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142582789	chr2:77855573-77855574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554065010	chr2:77855579-77855580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs4586656	chr2:77855589-77855590	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs536450835	chr2:77855612-77855613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368062085	chr2:77855634-77855635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs34932304	chr2:77855647-77855648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556776729	chr2:77855667-77855668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs202140468	chr2:77855686-77855687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs10865430	chr2:77855707-77855708	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs188194632	chr2:77855758-77855759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs557814146	chr2:77855824-77855825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs577796202	chr2:77855860-77855861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs149820905	chr2:77855890-77855891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs6726783	chr2:77855895-77855896	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs529034887	chr2:77855959-77855960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542464154	chr2:77855986-77855987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191542889	chr2:77856062-77856063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs145527892	chr2:77856082-77856083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547538343	chr2:77856102-77856103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551348497	chr2:77856160-77856161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs564980893	chr2:77856177-77856178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184092564	chr2:77856190-77856191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs375887464	chr2:77856201-77856202	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs189925484	chr2:77856234-77856235	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs182140253	chr2:77856239-77856240	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs536821148	chr2:77856292-77856293	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs550128861	chr2:77856311-77856312	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs187168835	chr2:77856317-77856318	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs34641691	chr2:77856328-77856329	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs539375099	chr2:77856355-77856356	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs370501690	chr2:77856356-77856357	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs561168605	chr2:77856394-77856395	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs12052760	chr2:77856415-77856416	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs577757189	chr2:77856554-77856555	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs552477638	chr2:77856565-77856566	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs62161511	chr2:77856619-77856620	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:59)

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

Chromatin state (count:226 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:77852800-77856800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:77854200-77857200	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr2:77854800-77856200	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr2:77854800-77856200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr2:77855000-77856200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:77855000-77856600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr2:77856200-77856400	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr2:77856200-77856400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr2:77856200-77856800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:77856200-77856800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr2:77856200-77857000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr2:77856200-77857400	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr2:77856400-77856800	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr2:77856400-77856800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr2:77856600-77857000	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr2:77856600-77857200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr2:77856600-77857200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr2:77856600-77857400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr2:77856600-77857400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr2:77856600-77857400	Enhancers	Fetal Heart	heart
21	chr2:77856600-77857400	Enhancers	HepG2	liver
22	chr2:77856800-77857000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr2:77856800-77857200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr2:77856800-77857200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr2:77856800-77857200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr2:77856800-77857200	Enhancers	Brain Hippocampus Middle	brain
27	chr2:77856800-77857400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr2:77856800-77857400	Enhancers	Brain Angular Gyrus	brain
29	chr2:77856800-77857400	Enhancers	Brain Cingulate Gyrus	brain
30	chr2:77856800-77857400	Enhancers	Brain Germinal Matrix	brain
31	chr2:77856800-77858200	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr2:77857000-77857200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr2:77857000-77857400	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr2:77857000-77857600	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr2:77857200-77857600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr2:77857200-77857600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:77857200-77857600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr2:77857400-77869400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr2:77860000-77861400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr2:77863400-77869200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr2:77869200-77869600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
42	chr2:77869400-77869800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr2:77869400-77870000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr2:77870000-77870600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
45	chr2:77877600-77878000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr2:77892000-77893800	Enhancers	Fetal Lung	lung
47	chr2:77892200-77894200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr2:77892800-77894000	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr2:77893200-77894200	Enhancers	HepG2	liver
50	chr2:77893600-77894200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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