Variant report

Variant	nsv588938
Chromosome Location	chr22:34270568-34307875
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:282)
CpG islands
(count:0)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:34305041-34305352	HepG2	liver:	n/a	n/a
2	ATF2	chr22:34291937-34293362	GM12878	blood:	n/a	n/a
3	ATF2	chr22:34292873-34293362	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr22:34292032-34292987	GM12878	blood:	n/a	n/a
5	BATF	chr22:34287933-34288315	GM12878	blood:	n/a	n/a
6	BATF	chr22:34292525-34293380	GM12878	blood:	n/a	chr22:34292610-34292623
7	BATF	chr22:34287968-34288282	GM12878	blood:	n/a	n/a
8	BATF	chr22:34291932-34292403	GM12878	blood:	n/a	chr22:34292191-34292202
9	BATF	chr22:34279533-34279901	GM12878	blood:	n/a	chr22:34279726-34279737
10	BATF	chr22:34279594-34279893	GM12878	blood:	n/a	chr22:34279726-34279737
11	BATF	chr22:34293029-34293343	GM12878	blood:	n/a	n/a
12	BCL11A	chr22:34279521-34279833	GM12878	blood:	n/a	n/a
13	BCL11A	chr22:34287951-34288299	GM12878	blood:	n/a	n/a
14	BCL11A	chr22:34279585-34279869	GM12878	blood:	n/a	n/a
15	BCL3	chr22:34287946-34288297	GM12878	blood:	n/a	n/a
16	BCL3	chr22:34279570-34279880	GM12878	blood:	n/a	n/a
17	BCLAF1	chr22:34291980-34293379	GM12878	blood:	n/a	chr22:34293008-34293017
18	BCLAF1	chr22:34285684-34286171	GM12878	blood:	n/a	n/a
19	BCLAF1	chr22:34292647-34293357	GM12878	blood:	n/a	chr22:34293008-34293017
20	BHLHE40	chr22:34291793-34292391	GM12878	blood:	n/a	n/a
21	CEBPB	chr22:34288655-34289018	HepG2	liver:	n/a	chr22:34288830-34288841 chr22:34288829-34288840
22	CEBPB	chr22:34287835-34288315	HepG2	liver:	n/a	chr22:34288136-34288147
23	CEBPB	chr22:34291813-34293124	GM12878	blood:	n/a	n/a
24	CEBPB	chr22:34287900-34288486	GM12878	blood:	n/a	chr22:34288136-34288147
25	CEBPB	chr22:34287957-34288301	IMR90	lung:	n/a	chr22:34288136-34288147
26	CEBPB	chr22:34306029-34306195	HepG2	liver:	n/a	chr22:34306126-34306139
27	CEBPB	chr22:34306017-34306297	IMR90	lung:	n/a	chr22:34306126-34306139
28	CHD1	chr22:34292833-34293122	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr22:34291632-34291696	GM12878	blood:	n/a	n/a
30	CTBP2	chr22:34292870-34293576	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr22:34288240-34288390	HepG2	liver:	n/a	n/a
32	CTCF	chr22:34277248-34277250	Medullo	brain:	n/a	n/a
33	CTCF	chr22:34293640-34293790	GM06990	blood:	n/a	n/a
34	CTCF	chr22:34293454-34293539	GM19239	blood:	n/a	n/a
35	CTCF	chr22:34277244-34277246	Medullo	brain:	n/a	n/a
36	CTCF	chr22:34271580-34271730	GM12873	blood:	n/a	n/a
37	CTCF	chr22:34294980-34295130	HL-60	blood:	n/a	n/a
38	CTCF	chr22:34292578-34292730	GM19239	blood:	n/a	n/a
39	CTCF	chr22:34292607-34292705	GM12892	blood:	n/a	n/a
40	CTCF	chr22:34272719-34272769	GM10248	blood:	n/a	n/a
41	CTCF	chr22:34277160-34277310	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr22:34277251-34277354	Medullo	brain:	n/a	n/a
43	CUX1	chr22:34285707-34285815	GM12878	blood:	n/a	n/a
44	CUX1	chr22:34288079-34288099	GM12878	blood:	n/a	n/a
45	E2F4	chr22:34285605-34285805	MCF10A-Er-Src	breast:	n/a	n/a
46	EBF1	chr22:34291389-34291695	GM12878	blood:	n/a	chr22:34291498-34291509
47	EBF1	chr22:34291263-34291714	GM12878	blood:	n/a	chr22:34291498-34291509
48	EBF1	chr22:34288110-34288478	GM12878	blood:	n/a	n/a
49	EBF1	chr22:34291325-34291677	GM12878	blood:	n/a	chr22:34291498-34291509
50	EBF1	chr22:34279604-34279996	GM12878	blood:	n/a	n/a

No data

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:34270428..34272649-chr22:34273804..34275941,2	MCF-7	breast:
2	chr22:34270428..34272649-chr22:34273804..34275941,2	MCF-7	breast:
3	chr22:34296334..34297959-chr22:34304595..34307456,3	MCF-7	breast:
4	chr22:34296231..34298036-chr22:34317275..34319526,2	MCF-7	breast:
5	chr22:34297092..34298993-chr22:34314365..34316257,2	MCF-7	breast:
6	chr22:34283903..34286858-chr22:34289207..34290909,2	MCF-7	breast:
7	chr22:34296334..34297959-chr22:34304595..34307456,3	MCF-7	breast:
8	chr22:34255630..34257426-chr22:34307549..34309607,2	MCF-7	breast:
9	chr22:34304733..34311493-chr22:34313014..34317407,8	MCF-7	breast:
10	chr22:34283913..34285789-chr22:34315526..34317915,2	MCF-7	breast:
11	chr22:34279207..34280839-chr22:34295025..34297477,2	MCF-7	breast:
12	chr22:34262180..34264985-chr22:34291444..34294296,2	MCF-7	breast:
13	chr22:34300595..34304253-chr22:34306616..34309764,3	MCF-7	breast:
14	chr22:34265653..34267240-chr22:34270322..34272194,2	MCF-7	breast:
15	chr22:34264153..34267717-chr22:34273021..34274940,3	MCF-7	breast:
16	chr22:34306645..34309140-chr22:34317602..34320390,2	MCF-7	breast:
17	chr22:34287867..34289464-chr22:34291655..34293352,2	MCF-7	breast:
18	chr22:34293649..34297424-chr22:34310921..34313948,3	MCF-7	breast:
19	chr22:34277917..34281628-chr22:34285820..34288664,3	MCF-7	breast:
20	chr22:34300595..34304253-chr22:34306616..34309764,3	MCF-7	breast:
21	chr22:34261283..34264105-chr22:34285527..34288136,2	MCF-7	breast:
22	chr22:34279207..34280839-chr22:34295025..34297477,2	MCF-7	breast:
23	chr22:34276961..34279522-chr22:34313897..34317110,3	MCF-7	breast:
24	chr22:34277917..34281628-chr22:34285820..34288664,3	MCF-7	breast:
25	chr22:34305108..34307624-chr22:34315419..34317424,2	MCF-7	breast:
26	chr22:34296673..34299632-chr22:34313962..34315661,2	MCF-7	breast:
27	chr22:34269817..34272444-chr22:34314882..34316654,2	MCF-7	breast:
28	chr22:34270457..34273179-chr22:34316799..34318425,2	MCF-7	breast:
29	chr22:34287867..34289464-chr22:34291655..34293352,2	MCF-7	breast:

No data

Variant related genes	Relation type
LARGE	TF binding region
ENSG00000273082	chromatin interactions
ENSG00000133424	chromatin interactions

Extended variants
information (count: 1566 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1566 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11705063	chr22:34270568-34270569	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113081723	chr22:34270573-34270574	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs16985378	chr22:34270618-34270619	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs62227815	chr22:34270620-34270621	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs141908644	chr22:34270628-34270629	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs367662948	chr22:34270636-34270637	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs59667917	chr22:34270665-34270666	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs5754734	chr22:34270693-34270694	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs150634906	chr22:34270699-34270700	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs544930747	chr22:34270722-34270723	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs557727011	chr22:34270818-34270819	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs578001842	chr22:34270913-34270914	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs540327154	chr22:34270933-34270934	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs186143808	chr22:34270940-34270941	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs111980830	chr22:34270953-34270954	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs543257171	chr22:34270979-34270980	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs563107040	chr22:34270980-34270981	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs538780990	chr22:34270982-34270983	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs190666045	chr22:34271025-34271026	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs564866983	chr22:34271070-34271071	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs558616637	chr22:34271158-34271159	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs369967174	chr22:34271192-34271193	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs527292229	chr22:34271239-34271240	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs547131417	chr22:34271262-34271263	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs567377203	chr22:34271263-34271264	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs182001542	chr22:34271271-34271272	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs553987270	chr22:34271325-34271326	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs28445256	chr22:34271333-34271334	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs549548980	chr22:34271392-34271393	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs75348684	chr22:34271409-34271410	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs186382244	chr22:34271420-34271421	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs115869922	chr22:34271427-34271428	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs577911243	chr22:34271440-34271441	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs534217451	chr22:34271494-34271495	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs553939570	chr22:34271499-34271500	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs146351315	chr22:34271500-34271501	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs543169263	chr22:34271531-34271532	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs76539250	chr22:34271601-34271602	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs9621794	chr22:34271618-34271619	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs556141613	chr22:34271627-34271628	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs73154546	chr22:34271689-34271690	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs190787303	chr22:34271701-34271702	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs377015634	chr22:34271734-34271735	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs9621795	chr22:34271782-34271783	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs547385731	chr22:34271812-34271813	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs183019630	chr22:34271823-34271824	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs144503478	chr22:34271854-34271855	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs144914991	chr22:34271855-34271856	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs188225554	chr22:34271930-34271931	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs538449115	chr22:34271939-34271940	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19384346	CNVD
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD
Deafness	17160897	CNVD
Bipolar disorder	19114987	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Prostate cancer	22341455	CNVD
Acute lymphoblastic leukemia	21339820	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

Chromatin state (count:872 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:34264000-34271200	Weak transcription	HSMM	muscle
2	chr22:34264800-34279400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr22:34265600-34271400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr22:34267600-34270600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr22:34267600-34271000	Enhancers	Primary B cells from peripheral blood	blood
6	chr22:34268000-34270600	Enhancers	Right Atrium	heart
7	chr22:34268000-34271400	Enhancers	Stomach Mucosa	stomach
8	chr22:34268000-34272600	Enhancers	H1 Cell Line	embryonic stem cell
9	chr22:34268800-34270800	Enhancers	Duodenum Mucosa	Duodenum
10	chr22:34269000-34270600	Enhancers	Ovary	ovary
11	chr22:34269000-34270600	Enhancers	Stomach Smooth Muscle	stomach
12	chr22:34269000-34271000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr22:34269000-34271600	Enhancers	Colonic Mucosa	Colon
14	chr22:34269000-34271800	Enhancers	HSMMtube	muscle
15	chr22:34269000-34272000	Enhancers	Colon Smooth Muscle	Colon
16	chr22:34269000-34272000	Enhancers	Duodenum Smooth Muscle	Duodenum
17	chr22:34269000-34272200	Enhancers	Fetal Lung	lung
18	chr22:34269000-34272200	Enhancers	Fetal Muscle Leg	muscle
19	chr22:34269000-34272400	Enhancers	Right Ventricle	heart
20	chr22:34269000-34273200	Enhancers	Brain Hippocampus Middle	brain
21	chr22:34269000-34273600	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr22:34269200-34270600	Enhancers	Brain Cingulate Gyrus	brain
23	chr22:34269200-34270600	Enhancers	Left Ventricle	heart
24	chr22:34269200-34270800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr22:34269200-34271000	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr22:34269200-34272200	Enhancers	Brain Anterior Caudate	brain
27	chr22:34269200-34272400	Enhancers	Fetal Brain Male	brain
28	chr22:34269200-34272600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr22:34269200-34272600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr22:34269200-34273000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr22:34269200-34273200	Enhancers	Brain Angular Gyrus	brain
32	chr22:34269200-34273800	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr22:34269400-34271000	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr22:34269400-34272400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr22:34269400-34272400	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr22:34269400-34272600	Enhancers	Psoas Muscle	Psoas
37	chr22:34269400-34273400	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr22:34269600-34270800	Weak transcription	Fetal Stomach	stomach
39	chr22:34269600-34271400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr22:34269600-34271600	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr22:34269600-34271800	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr22:34269600-34273600	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr22:34269800-34271200	Weak transcription	Adipose Nuclei	Adipose
44	chr22:34269800-34271200	Weak transcription	Fetal Brain Female	brain
45	chr22:34269800-34271200	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr22:34269800-34271200	Weak transcription	Spleen	Spleen
47	chr22:34269800-34271400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr22:34269800-34271400	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr22:34269800-34272200	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr22:34269800-34275400	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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