Variant report

Variant	esv6861
Chromosome Location	chr6:58774124-58777928
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:124)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:124 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:58777390..58779179-chr6:133135024..133136911,2	MCF-7	breast:
2	chr3:195577616..195578367-chr6:58777226..58778078,2	MCF-7	breast:
3	chr6:58777707..58778511-chr6:61909313..61909813,2	MCF-7	breast:
4	chr20:46129644..46132043-chr6:58777544..58779139,2	MCF-7	breast:
5	chr6:58776120..58778273-chr8:145699925..145701982,2	MCF-7	breast:
6	chr6:31782546..31783397-chr6:58777144..58777897,2	Hela-S3	cervix:
7	chr3:90450069..90451571-chr6:58776178..58778913,3	MCF-7	breast:
8	chr6:58776890..58777662-chr7:5569763..5570677,2	Hela-S3	cervix:
9	chr6:58777220..58778210-chr6:119855510..119856349,2	MCF-7	breast:
10	chr6:58777333..58777900-chr8:122346827..122347447,2	MCF-7	breast:
11	chr6:58777712..58778738-chr6:61909295..61909815,6	MCF-7	breast:
12	chr20:60960325..60962671-chr6:58777619..58780127,2	MCF-7	breast:
13	chr14:77757334..77757890-chr6:58776828..58777663,2	MCF-7	breast:
14	chr3:90451069..90451589-chr6:58776919..58777844,3	MCF-7	breast:
15	chr4:44423714..44424215-chr6:58777839..58778663,2	MCF-7	breast:
16	chr1:44683359..44684029-chr6:58777311..58778221,2	MCF-7	breast:
17	chr17:73716896..73718915-chr6:58776651..58778729,2	MCF-7	breast:
18	chr6:58775915..58778901-chr8:144691705..144693500,2	MCF-7	breast:
19	chr16:19191197..19191940-chr6:58777386..58777915,2	MCF-7	breast:
20	chr6:30581365..30583375-chr6:58776545..58779152,2	MCF-7	breast:
21	chr6:58776797..58778439-chr9:136323811..136326318,2	MCF-7	breast:
22	chr16:85495639..85498852-chr6:58775657..58778770,3	MCF-7	breast:
23	chr1:117112641..117113268-chr6:58775753..58776519,2	MCF-7	breast:
24	chr20:60877312..60877975-chr6:58777171..58777835,2	MCF-7	breast:
25	chr2:135217803..135218666-chr6:58777553..58778353,2	MCF-7	breast:
26	chr11:75291642..75294590-chr6:58777397..58779135,2	MCF-7	breast:
27	chr17:57920187..57922882-chr6:58774753..58776582,2	MCF-7	breast:
28	chr20:56089136..56089874-chr6:58774030..58774536,2	MCF-7	breast:
29	chr3:62439844..62440394-chr6:58777335..58777888,2	MCF-7	breast:
30	chr6:58773141..58775009-chr6:58776566..58778429,2	MCF-7	breast:
31	chr17:57697051..57699517-chr6:58775454..58778452,2	MCF-7	breast:
32	chr20:19348440..19350405-chr6:58776310..58778887,2	MCF-7	breast:
33	chr2:38304500..38306516-chr6:58776846..58778352,2	MCF-7	breast:
34	chr18:73688396..73689210-chr6:58777841..58778684,2	MCF-7	breast:
35	chr6:58776722..58778356-chr8:48323824..48325324,2	MCF-7	breast:
36	chr17:57920709..57924714-chr6:58775095..58779071,5	MCF-7	breast:
37	chr20:52327864..52329489-chr6:58775870..58778258,2	MCF-7	breast:
38	chr17:56707619..56709303-chr6:58776177..58777680,2	MCF-7	breast:
39	chr6:58772143..58775007-chr6:58776713..58778919,5	K562	blood:
40	chr12:6493660..6495635-chr6:58777646..58779181,2	MCF-7	breast:
41	chr1:201243876..201245779-chr6:58775647..58777227,2	MCF-7	breast:
42	chr12:80435495..80437852-chr6:58775102..58777367,2	MCF-7	breast:
43	chr11:58678524..58679504-chr6:58777166..58777745,2	MCF-7	breast:
44	chr12:38032912..38033432-chr6:58774035..58775015,2	MCF-7	breast:
45	chr5:157496471..157496971-chr6:58776705..58777406,2	MCF-7	breast:
46	chr20:52560026..52560620-chr6:58777219..58777738,2	MCF-7	breast:
47	chr20:45984506..45987023-chr6:58776231..58780015,3	MCF-7	breast:
48	chr20:62493089..62495109-chr6:58777340..58778920,2	MCF-7	breast:
49	chr12:117585721..117587663-chr6:58775712..58777632,2	MCF-7	breast:
50	chr1:216349276..216351630-chr6:58776732..58778763,2	MCF-7	breast:

No data

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

Extended variants
information (count: 1814 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1814 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386701816	chr6:58774150-58774151	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs185816389	chr6:58774188-58774189	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs4928481	chr6:58774189-58774190	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs9391449	chr6:58774199-58774200	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs577645199	chr6:58774201-58774202	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs545690968	chr6:58774202-58774203	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs77181706	chr6:58774206-58774207	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs572660892	chr6:58774209-58774210	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs76116853	chr6:58774210-58774211	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs568578578	chr6:58774214-58774215	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs528996693	chr6:58774218-58774219	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs78164468	chr6:58774227-58774228	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs550684062	chr6:58774245-58774246	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs9500406	chr6:58774249-58774250	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs556986648	chr6:58774250-58774251	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs112670963	chr6:58774255-58774256	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs533004203	chr6:58774256-58774257	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs9391450	chr6:58774261-58774262	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs79152584	chr6:58774270-58774271	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs74865803	chr6:58774276-58774277	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs386701818	chr6:58774280-58774281	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs116598362	chr6:58774281-58774282	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs534341231	chr6:58774283-58774284	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs143106186	chr6:58774289-58774290	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs553253455	chr6:58774291-58774292	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs115214755	chr6:58774297-58774298	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs567714600	chr6:58774298-58774299	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs537932770	chr6:58774300-58774301	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs573040763	chr6:58774301-58774302	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs116745002	chr6:58774302-58774303	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs542049696	chr6:58774303-58774304	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs556666663	chr6:58774306-58774307	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs80224997	chr6:58774317-58774318	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs370006957	chr6:58774318-58774319	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs555270261	chr6:58774322-58774323	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs76588756	chr6:58774326-58774327	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs6588719	chr6:58774327-58774328	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs6588720	chr6:58774328-58774329	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs373998233	chr6:58774331-58774332	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs572824189	chr6:58774363-58774364	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs183226080	chr6:58774390-58774391	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs370665589	chr6:58774394-58774395	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs74976581	chr6:58774395-58774396	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs540389619	chr6:58774399-58774400	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs58281759	chr6:58774409-58774410	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs78336389	chr6:58774414-58774415	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs57463413	chr6:58774420-58774421	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs386701819	chr6:58774432-58774433	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs62412777	chr6:58774434-58774435	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs28859614	chr6:58774440-58774441	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	Chromatin interactive region	2 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:312 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:58773400-58774800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr6:58773400-58774800	ZNF genes & repeats	Brain Hippocampus Middle	brain
3	chr6:58773400-58774800	ZNF genes & repeats	Colon Smooth Muscle	Colon
4	chr6:58773400-58774800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
5	chr6:58773400-58774800	ZNF genes & repeats	Fetal Lung	lung
6	chr6:58773400-58774800	ZNF genes & repeats	Rectal Smooth Muscle	rectum
7	chr6:58773400-58774800	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
8	chr6:58773400-58774800	ZNF genes & repeats	Stomach Smooth Muscle	stomach
9	chr6:58773400-58774800	ZNF genes & repeats	GM12878-XiMat	blood
10	chr6:58773400-58774800	ZNF genes & repeats	HUVEC	blood vessel
11	chr6:58773400-58775000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
12	chr6:58773400-58775000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr6:58773400-58775000	ZNF genes & repeats	Brain Anterior Caudate	brain
14	chr6:58773400-58775000	ZNF genes & repeats	Brain Cingulate Gyrus	brain
15	chr6:58773400-58775000	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
16	chr6:58773400-58775000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
17	chr6:58773400-58775000	ZNF genes & repeats	Dnd41	blood
18	chr6:58773400-58775200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr6:58773400-58775200	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr6:58773400-58775200	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
21	chr6:58773400-58775400	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
22	chr6:58773400-58775400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
23	chr6:58773400-58775600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
24	chr6:58773400-58775600	ZNF genes & repeats	Liver	Liver
25	chr6:58773400-58775800	ZNF genes & repeats	HMEC	breast
26	chr6:58773400-58776000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr6:58773400-58776000	ZNF genes & repeats	NH-A	brain
28	chr6:58773400-58776200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr6:58773400-58776200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
30	chr6:58773400-58776400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr6:58773400-58776400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
32	chr6:58773400-58776600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
33	chr6:58773400-58776600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
34	chr6:58773400-58776600	ZNF genes & repeats	Gastric	stomach
35	chr6:58773400-58776600	ZNF genes & repeats	Small Intestine	intestine
36	chr6:58773400-58779400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
37	chr6:58773400-58779400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr6:58773400-58779400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr6:58773400-58779400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
40	chr6:58773400-58779400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
41	chr6:58773400-58779400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
42	chr6:58773400-58779400	ZNF genes & repeats	Adipose Nuclei	Adipose
43	chr6:58773400-58779400	ZNF genes & repeats	Fetal Stomach	stomach
44	chr6:58773400-58779400	ZNF genes & repeats	Left Ventricle	heart
45	chr6:58773600-58774200	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
46	chr6:58773600-58774400	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
47	chr6:58773600-58774400	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
48	chr6:58773600-58774800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr6:58773600-58774800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr6:58773600-58774800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell

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