Variant report

Variant	esv6537
Chromosome Location	chr6:58776526-58779269
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:138)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:138 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:31782546..31783397-chr6:58777144..58777897,2	Hela-S3	cervix:
2	chr6:58776657..58777247-chrX:136737324..136737914,2	MCF-7	breast:
3	chr21:9826269..9827015-chr6:58776389..58777037,2	MCF-7	breast:
4	chr2:109819769..109820303-chr6:58776869..58777442,2	MCF-7	breast:
5	chr17:57914586..57918340-chr6:58776843..58780440,4	MCF-7	breast:
6	chr17:57920709..57924714-chr6:58775095..58779071,5	MCF-7	breast:
7	chr3:90451069..90451589-chr6:58776919..58777844,3	MCF-7	breast:
8	chr17:66287677..66288456-chr6:58778380..58779126,2	MCF-7	breast:
9	chr11:58678524..58679504-chr6:58777166..58777745,2	MCF-7	breast:
10	chr2:219259923..219262856-chr6:58776591..58778942,2	MCF-7	breast:
11	chr20:62493089..62495109-chr6:58777340..58778920,2	MCF-7	breast:
12	chr6:58777390..58779179-chr6:133135024..133136911,2	MCF-7	breast:
13	chr20:52815826..52816411-chr6:58777180..58778164,2	MCF-7	breast:
14	chr5:157496470..157497451-chr6:58776593..58777234,3	MCF-7	breast:
15	chr6:58777333..58777900-chr8:122346827..122347447,2	MCF-7	breast:
16	chr6:58776858..58779077-chr6:61908295..61909815,2	MCF-7	breast:
17	chr17:62622662..62623234-chr6:58778443..58779436,2	MCF-7	breast:
18	chr6:58776711..58777237-chr8:105771574..105772190,2	MCF-7	breast:
19	chr17:56736044..56736561-chr6:58778407..58779097,2	MCF-7	breast:
20	chr14:98326171..98326823-chr6:58778365..58778943,2	MCF-7	breast:
21	chr3:195577616..195578367-chr6:58777226..58778078,2	MCF-7	breast:
22	chr6:58777707..58778511-chr6:61909313..61909813,2	MCF-7	breast:
23	chr17:59628009..59628683-chr6:58777089..58777729,2	MCF-7	breast:
24	chr15:91473255..91473790-chr6:58778382..58779186,2	MCF-7	breast:
25	chr12:117585721..117587663-chr6:58775712..58777632,2	MCF-7	breast:
26	chr12:80435495..80437852-chr6:58775102..58777367,2	MCF-7	breast:
27	chr11:75291642..75294590-chr6:58777397..58779135,2	MCF-7	breast:
28	chr6:58773141..58775009-chr6:58776566..58778429,2	MCF-7	breast:
29	chr3:62439844..62440394-chr6:58777335..58777888,2	MCF-7	breast:
30	chr6:58776637..58777632-chr8:18871298..18871912,2	HCT-116	colon:
31	chr11:66445363..66446008-chr6:58776703..58777356,2	MCF-7	breast:
32	chr16:85495639..85498852-chr6:58775657..58778770,3	MCF-7	breast:
33	chr20:60877312..60877975-chr6:58777171..58777835,2	MCF-7	breast:
34	chr6:58772143..58775007-chr6:58776713..58778919,5	K562	blood:
35	chr20:19348440..19350405-chr6:58776310..58778887,2	MCF-7	breast:
36	chr17:57920187..57922882-chr6:58774753..58776582,2	MCF-7	breast:
37	chr6:58776953..58777924-chr9:126446426..126447140,2	MCF-7	breast:
38	chr10:90750069..90750688-chr6:58777473..58778220,2	Hela-S3	cervix:
39	chr22:32301912..32302764-chr6:58776740..58777661,2	MCF-7	breast:
40	chr17:57697051..57699517-chr6:58775454..58778452,2	MCF-7	breast:
41	chr6:58777220..58778210-chr6:119855510..119856349,2	MCF-7	breast:
42	chr4:26787771..26789874-chr6:58775360..58778093,2	MCF-7	breast:
43	chr1:9910788..9913768-chr6:58778329..58780695,2	MCF-7	breast:
44	chr6:58778355..58778904-chrX:56755266..56755790,2	MCF-7	breast:
45	chr17:56707689..56709464-chr6:58776179..58779153,2	MCF-7	breast:
46	chr6:30581365..30583375-chr6:58776545..58779152,2	MCF-7	breast:
47	chr17:56735441..56738187-chr6:58776197..58778735,2	MCF-7	breast:
48	chr3:63980131..63982580-chr6:58776275..58779243,2	MCF-7	breast:
49	chr6:58776676..58777225-chr8:72532546..72533088,2	MCF-7	breast:
50	chr3:16360548..16361058-chr6:58778316..58779058,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000122566	chromatin interactions
ENSG00000268858	chromatin interactions
ENSG00000184436	chromatin interactions
ENSG00000212017	chromatin interactions
ENSG00000101413	chromatin interactions
ENSG00000163635	chromatin interactions
ENSG00000248278	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000204389	chromatin interactions
ENSG00000246263	chromatin interactions
ENSG00000140553	chromatin interactions
ENSG00000207708	chromatin interactions
ENSG00000257084	chromatin interactions
ENSG00000124151	chromatin interactions
ENSG00000136997	chromatin interactions
ENSG00000104524	chromatin interactions
ENSG00000230513	chromatin interactions
ENSG00000168209	chromatin interactions
ENSG00000187013	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000101040	chromatin interactions
ENSG00000160325	chromatin interactions
ENSG00000122565	chromatin interactions
ENSG00000184348	chromatin interactions
ENSG00000207713	chromatin interactions
ENSG00000075624	chromatin interactions
ENSG00000255326	chromatin interactions
ENSG00000233822	chromatin interactions
ENSG00000204272	chromatin interactions
ENSG00000009830	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000171858	chromatin interactions
ENSG00000183665	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000160973	chromatin interactions
ENSG00000159202	chromatin interactions
ENSG00000089351	chromatin interactions
ENSG00000132470	chromatin interactions
ENSG00000204390	chromatin interactions
ENSG00000048392	chromatin interactions
ENSG00000206754	chromatin interactions
ENSG00000226137	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000203813	chromatin interactions
ENSG00000101407	chromatin interactions
ENSG00000175866	chromatin interactions
ENSG00000126749	chromatin interactions
ENSG00000141367	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000111321	chromatin interactions
ENSG00000103528	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000237080	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000185158	chromatin interactions
ENSG00000112306	chromatin interactions
ENSG00000026103	chromatin interactions
ENSG00000065135	chromatin interactions
ENSG00000173914	chromatin interactions
ENSG00000185650	chromatin interactions

Extended variants
information (count: 1670 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1670 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28823365	chr6:58776526-58776527	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
2	rs9391462	chr6:58776527-58776528	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
3	rs4454161	chr6:58776528-58776529	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
4	rs55658604	chr6:58776529-58776530	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
5	rs4524634	chr6:58776530-58776531	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
6	rs58357121	chr6:58776534-58776535	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
7	rs28844977	chr6:58776535-58776536	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
8	rs9377904	chr6:58776536-58776537	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
9	rs4395745	chr6:58776537-58776538	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
10	rs4524635	chr6:58776538-58776539	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
11	rs28804370	chr6:58776539-58776540	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
12	rs28803483	chr6:58776540-58776541	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
13	rs4555950	chr6:58776541-58776542	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
14	rs4524636	chr6:58776542-58776543	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
15	rs9404654	chr6:58776543-58776544	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
16	rs28790963	chr6:58776544-58776545	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
17	rs4928521	chr6:58776546-58776547	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
18	rs28871677	chr6:58776547-58776548	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
19	rs9377905	chr6:58776548-58776549	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
20	rs4476854	chr6:58776550-58776551	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
21	rs9500445	chr6:58776551-58776552	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
22	rs4317433	chr6:58776552-58776553	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
23	rs60774981	chr6:58776554-58776555	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
24	rs4928523	chr6:58776555-58776556	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
25	rs9391463	chr6:58776556-58776557	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
26	rs9500165	chr6:58776557-58776558	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
27	rs9377906	chr6:58776558-58776559	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
28	rs4615415	chr6:58776559-58776560	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
29	rs9391464	chr6:58776560-58776561	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
30	rs28786159	chr6:58776561-58776562	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
31	rs28895695	chr6:58776564-58776565	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
32	rs28813500	chr6:58776565-58776566	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
33	rs9500447	chr6:58776567-58776568	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
34	rs4928341	chr6:58776568-58776569	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
35	rs11961541	chr6:58776569-58776570	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
36	rs9500448	chr6:58776571-58776572	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
37	rs4569993	chr6:58776572-58776573	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
38	rs4549641	chr6:58776573-58776574	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
39	rs28851957	chr6:58776574-58776575	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
40	rs4433002	chr6:58776575-58776576	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
41	rs28819408	chr6:58776576-58776577	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
42	rs4928524	chr6:58776577-58776578	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
43	rs71275528	chr6:58776578-58776579	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
44	rs56923008	chr6:58776579-58776580	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
45	rs4394245	chr6:58776580-58776581	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
46	rs28773803	chr6:58776583-58776584	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
47	rs4530891	chr6:58776584-58776585	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
48	rs9500166	chr6:58776585-58776586	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
49	rs28799347	chr6:58776586-58776587	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
50	rs59313567	chr6:58776587-58776588	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	18458336	CNVD

Chromatin state (count:233 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:58773400-58776600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
2	chr6:58773400-58776600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
3	chr6:58773400-58776600	ZNF genes & repeats	Gastric	stomach
4	chr6:58773400-58776600	ZNF genes & repeats	Small Intestine	intestine
5	chr6:58773400-58779400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
6	chr6:58773400-58779400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:58773400-58779400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:58773400-58779400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
9	chr6:58773400-58779400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
10	chr6:58773400-58779400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
11	chr6:58773400-58779400	ZNF genes & repeats	Adipose Nuclei	Adipose
12	chr6:58773400-58779400	ZNF genes & repeats	Fetal Stomach	stomach
13	chr6:58773400-58779400	ZNF genes & repeats	Left Ventricle	heart
14	chr6:58773600-58776600	ZNF genes & repeats	Primary T cells from cord blood	blood
15	chr6:58773600-58776600	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr6:58773600-58779200	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
17	chr6:58773600-58779400	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
18	chr6:58773600-58779400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
19	chr6:58773600-58779400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
20	chr6:58773600-58779400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
21	chr6:58773600-58779400	ZNF genes & repeats	Primary B cells from cord blood	blood
22	chr6:58773600-58779400	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
23	chr6:58773600-58779400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr6:58773600-58779400	ZNF genes & repeats	Fetal Intestine Large	intestine
25	chr6:58774800-58776600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr6:58774800-58776600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr6:58774800-58776600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:58774800-58776600	Weak transcription	Primary B cells from peripheral blood	blood
29	chr6:58774800-58776600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr6:58774800-58776600	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr6:58774800-58776600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr6:58774800-58776600	Weak transcription	Brain Hippocampus Middle	brain
33	chr6:58774800-58776600	Weak transcription	Esophagus	oesophagus
34	chr6:58774800-58776600	Weak transcription	Fetal Brain Male	brain
35	chr6:58774800-58776600	Weak transcription	Fetal Heart	heart
36	chr6:58774800-58776600	Weak transcription	Fetal Kidney	kidney
37	chr6:58774800-58776600	Weak transcription	Placenta	Placenta
38	chr6:58774800-58776600	Weak transcription	Lung	lung
39	chr6:58774800-58776600	Weak transcription	Placenta Amnion	Placenta Amnion
40	chr6:58774800-58776600	Weak transcription	Right Atrium	heart
41	chr6:58774800-58776600	Weak transcription	Right Ventricle	heart
42	chr6:58774800-58776600	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr6:58774800-58776600	Weak transcription	Stomach Mucosa	stomach
44	chr6:58774800-58776600	Weak transcription	Stomach Smooth Muscle	stomach
45	chr6:58774800-58776600	Weak transcription	GM12878-XiMat	blood
46	chr6:58774800-58776600	Weak transcription	HUVEC	blood vessel
47	chr6:58774800-58776600	Weak transcription	K562	blood
48	chr6:58774800-58776600	Weak transcription	NHEK	skin
49	chr6:58774800-58776600	Weak transcription	Osteobl	bone
50	chr6:58775000-58776600	Weak transcription	Brain Substantia Nigra	brain

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