Variant report

Variant	nsv1009123
Chromosome Location	chr2:35728920-36412880
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1660)
CpG islands
(count:244)
Chromatin interactive
region (count:30)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1660 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:36392370-36392619	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:36214717-36214956	HepG2	liver:	n/a	n/a
3	ATF2	chr2:36374728-36375202	GM12878	blood:	n/a	n/a
4	BACH1	chr2:36246312-36246349	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:36163349-36163414	K562	blood:	n/a	n/a
6	BACH1	chr2:36180017-36180019	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr2:36374889-36375165	GM12878	blood:	n/a	n/a
8	BATF	chr2:36374886-36375226	GM12878	blood:	n/a	n/a
9	BCL11A	chr2:36374942-36375184	GM12878	blood:	n/a	chr2:36374970-36374979
10	BHLHE40	chr2:36214674-36215098	HepG2	liver:	n/a	n/a
11	BHLHE40	chr2:36411001-36411307	HepG2	liver:	n/a	n/a
12	BHLHE40	chr2:36115733-36115738	GM12878	blood:	n/a	n/a
13	BRCA1	chr2:36214839-36214902	HepG2	liver:	n/a	n/a
14	BRCA1	chr2:36285622-36285667	Hela-S3	cervix:	n/a	n/a
15	CCNT2	chr2:36229329-36229487	K562	blood:	n/a	n/a
16	CEBPB	chr2:36108892-36109092	Hela-S3	cervix:	n/a	chr2:36108992-36109003
17	CEBPB	chr2:36162107-36162428	IMR90	lung:	n/a	chr2:36162265-36162276
18	CEBPB	chr2:35939938-35940319	A549	lung:	n/a	n/a
19	CEBPB	chr2:35734480-35734730	A549	lung:	n/a	chr2:35734589-35734600
20	CEBPB	chr2:35748868-35749205	IMR90	lung:	n/a	chr2:35749027-35749038
21	CEBPB	chr2:35849689-35849697	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr2:35772172-35772385	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:35933608-35933969	HepG2	liver:	n/a	chr2:35933776-35933785 chr2:35933774-35933785 chr2:35933776-35933787
24	CEBPB	chr2:35923382-35923646	HepG2	liver:	n/a	chr2:35923513-35923522 chr2:35923513-35923524 chr2:35923491-35923502 chr2:35923511-35923522 chr2:35923511-35923524
25	CEBPB	chr2:35734448-35734766	HepG2	liver:	n/a	chr2:35734589-35734600
26	CEBPB	chr2:35728741-35729438	Hela-S3	cervix:	n/a	chr2:35729241-35729252 chr2:35729241-35729254
27	CEBPB	chr2:36375180-36375486	A549	lung:	n/a	n/a
28	CEBPB	chr2:35966667-35966899	IMR90	lung:	n/a	n/a
29	CEBPB	chr2:36068970-36069119	IMR90	lung:	n/a	chr2:36069021-36069032
30	CEBPB	chr2:35933490-35933969	Hela-S3	cervix:	n/a	chr2:35933776-35933785 chr2:35933774-35933785 chr2:35933776-35933787
31	CEBPB	chr2:35933609-35933948	IMR90	lung:	n/a	chr2:35933776-35933785 chr2:35933774-35933785 chr2:35933776-35933787
32	CEBPB	chr2:36106683-36106761	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:36052197-36052252	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:36162102-36162418	HepG2	liver:	n/a	chr2:36162265-36162276
35	CEBPB	chr2:36354969-36355117	HepG2	liver:	n/a	chr2:36355034-36355045
36	CEBPB	chr2:35763050-35763245	A549	lung:	n/a	n/a
37	CEBPB	chr2:36044031-36044069	HepG2	liver:	n/a	chr2:36044042-36044055 chr2:36044042-36044055
38	CEBPB	chr2:36162133-36162426	H1-hESC	embryonic stem cell:	n/a	chr2:36162265-36162276
39	CEBPB	chr2:36137484-36137491	HepG2	liver:	n/a	n/a
40	CEBPB	chr2:36379312-36379579	HepG2	liver:	n/a	chr2:36379457-36379468
41	CEBPB	chr2:36106593-36106880	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr2:36000495-36000514	HepG2	liver:	n/a	chr2:36000495-36000506
43	CEBPB	chr2:35939980-35940327	K562	blood:	n/a	n/a
44	CEBPB	chr2:36195167-36195440	HepG2	liver:	n/a	chr2:36195276-36195287
45	CEBPB	chr2:36214637-36214840	HepG2	liver:	n/a	chr2:36214741-36214754 chr2:36214741-36214754 chr2:36214741-36214752
46	CEBPB	chr2:36214633-36214927	Hela-S3	cervix:	n/a	chr2:36214741-36214754 chr2:36214741-36214754 chr2:36214741-36214752
47	CEBPB	chr2:36156290-36156470	A549	lung:	n/a	n/a
48	CEBPB	chr2:36106619-36106946	MCF-7	breast:	n/a	n/a
49	CEBPB	chr2:35933609-35933943	H1-hESC	embryonic stem cell:	n/a	chr2:35933776-35933785 chr2:35933774-35933785 chr2:35933776-35933787
50	CEBPB	chr2:36214004-36214091	A549	lung:	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	chr2:36406592-36406642	HMEC	breast:	n/a
2	chr2:36157995-36158045	Hela-S3	cervix:	n/a
3	chr2:36157995-36158045	HAEpiC	amniotic membrane:	n/a
4	chr2:36018275-36018325	LNCaP	prostate:	n/a
5	chr2:36049853-36049903	PFSK-1	brain:	n/a
6	chr2:36406592-36406642	SK-N-MC	brain:	n/a
7	chr2:36049853-36049903	PrEC	prostate:	n/a
8	chr2:36049853-36049903	NHDF-neo	bronchial:	n/a
9	chr2:36157995-36158045	HRPEpiC	eye:	n/a
10	chr2:36049853-36049903	HCF	heart:	n/a
11	chr2:36157995-36158045	SAEC	small airway:	n/a
12	chr2:36157995-36158045	GM12892	blood:	n/a
13	chr2:36157995-36158045	SK-N-SH_RA	brain:	n/a
14	chr2:36406592-36406642	Jurkat	blood:	n/a
15	chr2:36157995-36158045	ProgFib	skin:	n/a
16	chr2:36049853-36049903	SK-N-SH_RA	brain:	n/a
17	chr2:36018275-36018325	ECC-1	luminal epithelium:	n/a
18	chr2:36157995-36158045	K562	blood:	n/a
19	chr2:36049853-36049903	GM19239	blood:	n/a
20	chr2:36018275-36018325	GM12878	blood:	n/a
21	chr2:36157995-36158045	HRE	kidney:	n/a
22	chr2:36049853-36049903	SK-N-MC	brain:	n/a
23	chr2:36406592-36406642	GM12891	blood:	n/a
24	chr2:36406592-36406642	NHDF-neo	bronchial:	n/a
25	chr2:36018275-36018325	HAEpiC	amniotic membrane:	n/a
26	chr2:36049853-36049903	AG04450	lung:	fetal
27	chr2:36018275-36018325	Hepatocyte	liver:	n/a
28	chr2:36406592-36406642	HEEpiC	esophagus:	n/a
29	chr2:36049853-36049903	ProgFib	skin:	n/a
30	chr2:36157995-36158045	NHDF-neo	bronchial:	n/a
31	chr2:36049853-36049903	HRCEpiC	kidney:	n/a
32	chr2:36406592-36406642	HCM	heart:	n/a
33	chr2:36406592-36406642	SK-N-SH	brain:	n/a
34	chr2:36406592-36406642	RPTEC	kidney:	n/a
35	chr2:36157995-36158045	LNCaP	prostate:	n/a
36	chr2:36157995-36158045	Caco-2	colon:	n/a
37	chr2:36157995-36158045	GM12878	blood:	n/a
38	chr2:36406592-36406642	AG04449	skin:	fetal
39	chr2:36157995-36158045	GM19239	blood:	n/a
40	chr2:36049853-36049903	HCT-116	colon:	n/a
41	chr2:36406592-36406642	HPAEpiC	pulmonary alveolar:	n/a
42	chr2:36018275-36018325	NH-A	brain:	n/a
43	chr2:36406592-36406642	AG04450	lung:	fetal
44	chr2:36049853-36049903	AG09309	skin:	n/a
45	chr2:36049853-36049903	GM06990	blood:	n/a
46	chr2:36018275-36018325	GM19239	blood:	n/a
47	chr2:36018275-36018325	SK-N-SH_RA	brain:	n/a
48	chr2:36157995-36158045	HPAEpiC	pulmonary alveolar:	n/a
49	chr2:36157995-36158045	AG09319	gingival:	n/a
50	chr2:36018275-36018325	MCF-7	breast:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:36243496..36245168-chr2:36248339..36251225,2	K562	blood:
2	chr2:35877173..35880679-chr2:35885712..35889508,3	MCF-7	breast:
3	chr2:36243496..36245168-chr2:36248339..36251225,2	K562	blood:
4	chr2:36099243..36100067-chr2:36734209..36735134,2	MCF-7	breast:
5	chr2:36208827..36211193-chr2:36213089..36216018,2	MCF-7	breast:
6	chr2:36262623..36264860-chr2:36265182..36267594,2	K562	blood:
7	chr2:36375898..36378508-chr2:36382841..36384658,2	K562	blood:
8	chr2:36026668..36029472-chr2:36034547..36037398,2	K562	blood:
9	chr2:35878984..35880554-chr2:35880811..35883619,2	K562	blood:
10	chr2:36167966..36170859-chr2:36172337..36174849,2	MCF-7	breast:
11	chr2:35878984..35880554-chr2:35880811..35883619,2	K562	blood:
12	chr2:36198079..36198752-chr2:36549195..36549978,3	MCF-7	breast:
13	chr2:36208827..36211193-chr2:36213089..36216018,2	MCF-7	breast:
14	chr14:33621149..33624012-chr2:35726795..35729641,2	MCF-7	breast:
15	chr2:35887668..35890004-chr2:35892119..35894663,2	K562	blood:
16	chr2:36346980..36349018-chr2:36352266..36354440,2	K562	blood:
17	chr2:36167966..36170859-chr2:36172337..36174849,2	MCF-7	breast:
18	chr2:36375898..36378508-chr2:36382841..36384658,2	K562	blood:
19	chr2:35949877..35953265-chr2:35954228..35956588,3	MCF-7	breast:
20	chr2:35847208..35849274-chr2:35852737..35854636,2	K562	blood:
21	chr2:36026668..36029472-chr2:36034547..36037398,2	K562	blood:
22	chr2:35863760..35866047-chr2:35869717..35871925,2	MCF-7	breast:
23	chr2:35847208..35849274-chr2:35852737..35854636,2	K562	blood:
24	chr2:36222475..36223224-chr6:31509383..31509944,2	MCF-7	breast:
25	chr2:35877173..35880679-chr2:35885712..35889508,3	MCF-7	breast:
26	chr2:35863760..35866047-chr2:35869717..35871925,2	MCF-7	breast:
27	chr2:36346980..36349018-chr2:36352266..36354440,2	K562	blood:
28	chr2:36262623..36264860-chr2:36265182..36267594,2	K562	blood:
29	chr2:35887668..35890004-chr2:35892119..35894663,2	K562	blood:
30	chr2:36198095..36199022-chr2:36584804..36585700,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC007401.2.1-6	chr2:35949825-35950208	NONHSAT070075

No data

Variant related genes	Relation type
MRPL50P1	TF binding region
MRPL50P1	CpG island
ENSG00000234587	chromatin interactions
ENSG00000198563	chromatin interactions

Extended variants
information (count: 16821 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:16821 , 50 per page) page: 1 2 3 4 5 6 7 ... 337

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11124446	chr2:35728942-35728943	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs561464426	chr2:35728964-35728965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576682716	chr2:35729036-35729037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559440219	chr2:35729046-35729047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs140471210	chr2:35729054-35729055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533054485	chr2:35729095-35729096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185355123	chr2:35729137-35729138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs111788294	chr2:35729216-35729217	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs374072174	chr2:35729232-35729233	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs544812411	chr2:35729233-35729234	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs376699175	chr2:35729264-35729265	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs563478183	chr2:35729273-35729274	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs530641604	chr2:35729290-35729291	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs373261832	chr2:35729313-35729314	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs57865658	chr2:35729335-35729336	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs567232516	chr2:35729399-35729400	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs191782517	chr2:35729425-35729426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs6717672	chr2:35729475-35729476	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs143659604	chr2:35729495-35729496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs6731097	chr2:35729513-35729514	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs557200714	chr2:35729514-35729515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569402376	chr2:35729515-35729516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536458579	chr2:35729517-35729518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs555201466	chr2:35729522-35729523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs7607623	chr2:35729556-35729557	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
26	rs540971526	chr2:35729559-35729560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs148166808	chr2:35729566-35729567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183251652	chr2:35729577-35729578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545060768	chr2:35729583-35729584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372841797	chr2:35729597-35729598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563255983	chr2:35729598-35729599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530690828	chr2:35729653-35729654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs76183653	chr2:35729673-35729674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs374906226	chr2:35729674-35729675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560795207	chr2:35729678-35729679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528361015	chr2:35729691-35729692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs567307169	chr2:35729692-35729693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377256838	chr2:35729710-35729711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs74787247	chr2:35729718-35729719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs532420672	chr2:35729760-35729761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs527540587	chr2:35729764-35729765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551017789	chr2:35729795-35729796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11887298	chr2:35729869-35729870	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs74930392	chr2:35729871-35729872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs548793196	chr2:35729881-35729882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567107318	chr2:35729899-35729900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538148862	chr2:35729915-35729916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534475310	chr2:35729967-35729968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188028677	chr2:35729981-35729982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs199543814	chr2:35729990-35729991	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	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
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Autism	22495309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:666 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:35728000-35730000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:35728200-35730400	Enhancers	HMEC	breast
3	chr2:35728400-35729800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr2:35728400-35729800	Enhancers	Hela-S3	cervix
5	chr2:35728600-35729800	Enhancers	NHEK	skin
6	chr2:35728800-35729200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:35728800-35729200	Enhancers	HUVEC	blood vessel
8	chr2:35729200-35729400	Flanking Active TSS	HUVEC	blood vessel
9	chr2:35729200-35730400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr2:35729400-35730400	Enhancers	HUVEC	blood vessel
11	chr2:35730400-35733600	Weak transcription	HUVEC	blood vessel
12	chr2:35730400-35735600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr2:35730400-35735600	Weak transcription	HMEC	breast
14	chr2:35733600-35735600	Enhancers	HUVEC	blood vessel
15	chr2:35735600-35736200	Flanking Active TSS	HUVEC	blood vessel
16	chr2:35735600-35736400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr2:35735600-35736400	Enhancers	HMEC	breast
18	chr2:35735800-35736200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr2:35735800-35736200	Enhancers	Adipose Nuclei	Adipose
20	chr2:35735800-35736400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr2:35736200-35736800	Enhancers	HUVEC	blood vessel
22	chr2:35736400-35739800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr2:35739800-35740200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr2:35741000-35743000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr2:35743000-35743800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
26	chr2:35743800-35747600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr2:35743800-35754600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr2:35747000-35748000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr2:35747000-35748200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr2:35747000-35748200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr2:35747200-35747800	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr2:35747200-35748000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr2:35747600-35748000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr2:35747800-35748200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr2:35747800-35748400	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr2:35748200-35749000	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr2:35754600-35755000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr2:35754600-35755000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
39	chr2:35755000-35757400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr2:35755800-35756200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr2:35764000-35764600	Enhancers	HMEC	breast
42	chr2:35764200-35764800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr2:35764600-35766400	Weak transcription	HMEC	breast
44	chr2:35766400-35766800	Enhancers	HMEC	breast
45	chr2:35771000-35771600	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr2:35781000-35781800	Enhancers	Pancreas	Pancrea
47	chr2:35794400-35795200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr2:35800000-35800800	Enhancers	Pancreas	Pancrea
49	chr2:35800200-35800600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr2:35800800-35803200	Weak transcription	Pancreas	Pancrea

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