Variant report

Variant	nsv916310
Chromosome Location	chr12:84589526-84815067
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	chr12:84666195-84666238	K562	blood:	n/a	n/a
2	ATF2	chr12:84814877-84815301	GM12878	blood:	n/a	n/a
3	ATF2	chr12:84814820-84815329	GM12878	blood:	n/a	n/a
4	BACH1	chr12:84703758-84703952	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr12:84814927-84815259	GM12878	blood:	n/a	n/a
6	BATF	chr12:84814851-84815197	GM12878	blood:	n/a	n/a
7	BCL11A	chr12:84814922-84815248	GM12878	blood:	n/a	chr12:84815094-84815103
8	BCL11A	chr12:84814960-84815161	GM12878	blood:	n/a	chr12:84815094-84815103
9	BRCA1	chr12:84760808-84760827	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr12:84773793-84774149	IMR90	lung:	n/a	chr12:84773956-84773967
11	CEBPB	chr12:84773812-84774129	HepG2	liver:	n/a	chr12:84773956-84773967
12	CEBPB	chr12:84810437-84810903	Hela-S3	cervix:	n/a	chr12:84810438-84810449
13	CEBPB	chr12:84735646-84735920	A549	lung:	n/a	chr12:84735771-84735782
14	CEBPB	chr12:84735633-84735950	HepG2	liver:	n/a	chr12:84735771-84735782
15	CEBPB	chr12:84735640-84735903	K562	blood:	n/a	chr12:84735771-84735782
16	CEBPB	chr12:84705099-84705356	HepG2	liver:	n/a	n/a
17	CEBPB	chr12:84754178-84754417	Hela-S3	cervix:	n/a	chr12:84754301-84754312
18	CEBPB	chr12:84773850-84774062	K562	blood:	n/a	chr12:84773956-84773967
19	CEBPB	chr12:84735626-84735910	Hela-S3	cervix:	n/a	chr12:84735771-84735782
20	CEBPB	chr12:84735641-84735936	H1-hESC	embryonic stem cell:	n/a	chr12:84735771-84735782
21	CEBPB	chr12:84773957-84774038	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr12:84783579-84783909	HepG2	liver:	n/a	chr12:84783756-84783767
23	CEBPB	chr12:84754179-84754409	HepG2	liver:	n/a	chr12:84754301-84754312
24	CEBPB	chr12:84760167-84760367	K562	blood:	n/a	chr12:84760300-84760313 chr12:84760328-84760337 chr12:84760167-84760180 chr12:84760326-84760339 chr12:84760326-84760337 chr12:84760326-84760339
25	CEBPB	chr12:84773813-84774129	A549	lung:	n/a	chr12:84773956-84773967
26	CEBPB	chr12:84735587-84735953	IMR90	lung:	n/a	chr12:84735771-84735782
27	CEBPB	chr12:84612277-84612494	MCF-7	breast:	n/a	chr12:84612397-84612410
28	CEBPB	chr12:84612283-84612492	A549	lung:	n/a	chr12:84612397-84612410
29	CHD2	chr12:84752859-84752895	HepG2	liver:	n/a	n/a
30	CTCF	chr12:84739454-84739538	GM13976	blood:	n/a	n/a
31	CTCF	chr12:84791011-84791526	HCT-116	colon:	n/a	chr12:84791277-84791284 chr12:84791271-84791287 chr12:84791265-84791286 chr12:84791270-84791288
32	CTCF	chr12:84810527-84810530	K562	blood:	n/a	n/a
33	CTCF	chr12:84634200-84634350	AG04450	lung:	n/a	n/a
34	CTCF	chr12:84791180-84791330	AG04449	skin:	n/a	chr12:84791277-84791284 chr12:84791271-84791287 chr12:84791265-84791286 chr12:84791270-84791288
35	CTCF	chr12:84791220-84791370	HMF	breast:	n/a	chr12:84791277-84791284 chr12:84791271-84791287 chr12:84791265-84791286 chr12:84791270-84791288
36	CTCF	chr12:84791200-84791350	BJ	skin:	n/a	chr12:84791277-84791284 chr12:84791271-84791287 chr12:84791265-84791286 chr12:84791270-84791288
37	CTCF	chr12:84791020-84791170	HFF	foreskin:	n/a	n/a
38	CTCF	chr12:84703860-84704010	NHEK	skin:	n/a	n/a
39	CTCF	chr12:84791198-84791352	LNCaP	prostate:	n/a	chr12:84791277-84791284 chr12:84791271-84791287 chr12:84791265-84791286 chr12:84791270-84791288
40	CTCF	chr12:84791060-84791210	AG04450	lung:	n/a	n/a
41	CTCF	chr12:84791140-84791290	SK-N-SH_RA	brain:	n/a	chr12:84791277-84791284 chr12:84791271-84791287 chr12:84791265-84791286 chr12:84791270-84791288
42	CTCF	chr12:84791220-84791370	AG10803	skin:	n/a	chr12:84791277-84791284 chr12:84791271-84791287 chr12:84791265-84791286 chr12:84791270-84791288
43	CTCF	chr12:84791240-84791390	WI-38	lung:	n/a	chr12:84791277-84791284 chr12:84791271-84791287 chr12:84791265-84791286 chr12:84791270-84791288
44	CTCF	chr12:84791140-84791290	HA-sp	spinal cord:	n/a	chr12:84791277-84791284 chr12:84791271-84791287 chr12:84791265-84791286 chr12:84791270-84791288
45	CTCF	chr12:84791220-84791370	SAEC	small airway:	n/a	chr12:84791277-84791284 chr12:84791271-84791287 chr12:84791265-84791286 chr12:84791270-84791288
46	CTCF	chr12:84791254-84791348	Hela-S3	cervix:	n/a	chr12:84791277-84791284 chr12:84791271-84791287 chr12:84791265-84791286 chr12:84791270-84791288
47	CTCF	chr12:84603895-84603920	MCF-7	breast:	n/a	n/a
48	CTCF	chr12:84791000-84791150	BE2_C	brain:	n/a	n/a
49	CTCF	chr12:84791160-84791310	SAEC	small airway:	n/a	chr12:84791277-84791284 chr12:84791271-84791287 chr12:84791265-84791286 chr12:84791270-84791288
50	CTCF	chr12:84791220-84791370	AG04449	skin:	n/a	chr12:84791277-84791284 chr12:84791271-84791287 chr12:84791265-84791286 chr12:84791270-84791288

No.	Distal block	Cell Line	Cell type
1	chr12:84592646..84594505-chr12:84594640..84596287,2	MCF-7	breast:
2	chr12:84611922..84614915-chr12:84630882..84632480,2	MCF-7	breast:
3	chr12:84219094..84220507-chr12:84790896..84791617,3	MCF-7	breast:
4	chr12:84754965..84757723-chr12:84759689..84762304,2	MCF-7	breast:
5	chr12:84611922..84614915-chr12:84630882..84632480,2	MCF-7	breast:
6	chr12:84754965..84757723-chr12:84759689..84762304,2	MCF-7	breast:
7	chr12:84600531..84602051-chr6:31495165..31496871,2	K562	blood:
8	chr12:84219617..84220155-chr12:84790822..84791366,2	MCF-7	breast:
9	chr12:84677376..84680215-chr12:84681765..84683893,2	K562	blood:
10	chr12:84596837..84598758-chr12:84604233..84606547,2	MCF-7	breast:
11	chr12:84814316..84817174-chr12:84818973..84820738,2	MCF-7	breast:
12	chr12:84592646..84594505-chr12:84594640..84596287,2	MCF-7	breast:
13	chr12:84615761..84617587-chr14:52985387..52988384,2	MCF-7	breast:
14	chr12:84596837..84598758-chr12:84604233..84606547,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRIQ1-2	chr12:84687707-84687920	ENSG00000257729
2	lnc-LRRIQ1-2	chr12:84678170-84678273	ENSG00000257729
3	lnc-LRRIQ1-2	chr12:84688089-84688341	ENSG00000257729
4	lnc-LRRIQ1-2	chr12:84688089-84688335	ENSG00000257729
5	lnc-LRRIQ1-2	chr12:84665119-84665185	ENSG00000257729

Variant related genes	Relation type
ENSG00000257729	TF binding region
ENSG00000257729	chromatin interactions
ENSG00000204511	chromatin interactions
ENSG00000225499	chromatin interactions

Extended variants
information (count: 2047 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2047 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143870334	chr12:84600551-84600552	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs183649876	chr12:84600569-84600570	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs146306643	chr12:84600616-84600617	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs555794523	chr12:84600632-84600633	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs139143859	chr12:84600634-84600635	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs543834340	chr12:84600638-84600639	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs555725658	chr12:84600678-84600679	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs78446903	chr12:84600684-84600685	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs544774097	chr12:84600748-84600749	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs560149818	chr12:84600790-84600791	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs188528653	chr12:84600794-84600795	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs2929815	chr12:84600810-84600811	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs149366020	chr12:84600829-84600830	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs531611898	chr12:84600833-84600834	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs368032830	chr12:84600859-84600860	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs541401735	chr12:84600868-84600869	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs561290199	chr12:84600872-84600873	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs192829618	chr12:84600909-84600910	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs562857973	chr12:84600938-84600939	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs78980645	chr12:84600980-84600981	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs551587461	chr12:84601012-84601013	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs566916434	chr12:84601018-84601019	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs534144434	chr12:84601033-84601034	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs373217012	chr12:84601052-84601053	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs567653672	chr12:84601065-84601066	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs538140297	chr12:84601073-84601074	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs555787122	chr12:84601123-84601124	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs577225444	chr12:84601149-84601150	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs7956052	chr12:84601156-84601157	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs183020037	chr12:84601236-84601237	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs75367574	chr12:84601241-84601242	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs542482902	chr12:84601256-84601257	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs370563343	chr12:84601267-84601268	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs73164233	chr12:84601319-84601320	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs530326064	chr12:84601341-84601342	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs144727969	chr12:84601397-84601398	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs74106414	chr12:84601400-84601401	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs371925198	chr12:84601429-84601430	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs386377188	chr12:84601430-84601431	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs71072041	chr12:84601447-84601448	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs2929816	chr12:84601450-84601451	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs563866045	chr12:84601479-84601480	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs531286713	chr12:84601524-84601525	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs551717346	chr12:84601572-84601573	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs560403379	chr12:84601581-84601582	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs148572045	chr12:84601598-84601599	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs549353545	chr12:84601617-84601618	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs567518440	chr12:84601623-84601624	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs370927835	chr12:84601629-84601630	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs186568591	chr12:84601634-84601635	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:84605400-84605800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr12:84653800-84654000	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr12:84654000-84655000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr12:84655000-84655800	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr12:84658400-84658800	Enhancers	Fetal Brain Male	brain
6	chr12:84658800-84659200	Weak transcription	Fetal Brain Male	brain
7	chr12:84659200-84659800	Enhancers	Fetal Brain Male	brain
8	chr12:84662200-84664000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr12:84663800-84664200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
10	chr12:84663800-84664400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
11	chr12:84663800-84665200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
12	chr12:84664000-84664200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr12:84664000-84664400	Enhancers	NHEK	skin
14	chr12:84664000-84664600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
15	chr12:84664000-84665400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr12:84664200-84664400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
17	chr12:84664200-84664400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
18	chr12:84664200-84664800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr12:84664200-84664800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
20	chr12:84664200-84664800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr12:84664200-84665000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
22	chr12:84664200-84665000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:84664400-84664800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
24	chr12:84664400-84664800	Flanking Active TSS	NHEK	skin
25	chr12:84664400-84665200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr12:84664600-84664800	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
27	chr12:84664600-84664800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
28	chr12:84664600-84664800	Enhancers	H9 Cell Line	embryonic stem cell
29	chr12:84664600-84665000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr12:84664600-84665000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
31	chr12:84664800-84665000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
32	chr12:84664800-84665000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr12:84664800-84665200	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
34	chr12:84664800-84665200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
35	chr12:84664800-84665200	Enhancers	NHEK	skin
36	chr12:84665000-84665200	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
37	chr12:84665000-84665200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr12:84665200-84670000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr12:84670000-84670200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr12:84678200-84679000	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr12:84679400-84679800	Enhancers	NHEK	skin
42	chr12:84683800-84684600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr12:84683800-84685000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr12:84684000-84684600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr12:84698800-84699200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr12:84698800-84699400	Enhancers	Fetal Lung	lung
47	chr12:84698800-84699600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr12:84706800-84707200	Enhancers	Fetal Lung	lung
49	chr12:84719400-84720400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr12:84719800-84720200	Enhancers	iPS-18 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links