Variant report

Variant	esv2440024
Chromosome Location	chr6:58773927-58778724
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:142)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:142 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:58778318..58779144-chr9:130843661..130844171,2	MCF-7	breast:
2	chr13:111364963..111367929-chr6:58777252..58779728,2	MCF-7	breast:
3	chr6:58772384..58775379-chr6:58777406..58779060,3	K562	blood:
4	chr3:90451071..90451591-chr6:58777202..58777887,2	MCF-7	breast:
5	chr6:31849956..31851616-chr6:58776203..58778751,2	MCF-7	breast:
6	chr20:46135534..46137185-chr6:58775644..58777423,2	MCF-7	breast:
7	chr14:19023553..19024073-chr6:58778553..58779079,2	MCF-7	breast:
8	chr18:73688396..73689210-chr6:58777841..58778684,2	MCF-7	breast:
9	chr11:58677524..58679024-chr6:58777164..58778728,2	K562	blood:
10	chr6:58776666..58779159-chr8:125462787..125464378,2	MCF-7	breast:
11	chr20:60877312..60877975-chr6:58777171..58777835,2	MCF-7	breast:
12	chr3:62439844..62440394-chr6:58777335..58777888,2	MCF-7	breast:
13	chr6:58776637..58777632-chr8:18871298..18871912,2	HCT-116	colon:
14	chr18:55334307..55335255-chr6:58777372..58777917,2	MCF-7	breast:
15	chr4:26787771..26789874-chr6:58775360..58778093,2	MCF-7	breast:
16	chr17:57928094..57930742-chr6:58776120..58778676,4	MCF-7	breast:
17	chr17:56735441..56738187-chr6:58776197..58778735,2	MCF-7	breast:
18	chr6:58778414..58779270-chr7:26240803..26241518,2	Hela-S3	cervix:
19	chr4:44423714..44424215-chr6:58777839..58778663,2	MCF-7	breast:
20	chr17:46984708..46987154-chr6:58777011..58778755,2	MCF-7	breast:
21	chr11:66445363..66446008-chr6:58776703..58777356,2	MCF-7	breast:
22	chr20:36661511..36663112-chr6:58773928..58776889,2	K562	blood:
23	chr6:58778355..58778904-chrX:56755266..56755790,2	MCF-7	breast:
24	chr2:109819769..109820303-chr6:58776869..58777442,2	MCF-7	breast:
25	chr14:70592691..70594528-chr6:58777109..58778754,2	MCF-7	breast:
26	chr14:19022553..19024053-chr6:58774785..58777168,2	MCF-7	breast:
27	chr6:58776711..58777237-chr8:105771574..105772190,2	MCF-7	breast:
28	chr6:58775076..58778073-chr8:103250732..103252303,2	K562	blood:
29	chr17:57920709..57924714-chr6:58775095..58779071,5	MCF-7	breast:
30	chr17:57914586..57918340-chr6:58776843..58780440,4	MCF-7	breast:
31	chr20:52815826..52816411-chr6:58777180..58778164,2	MCF-7	breast:
32	chr6:58777333..58777900-chr8:122346827..122347447,2	MCF-7	breast:
33	chr3:90451069..90451589-chr6:58776919..58777844,3	MCF-7	breast:
34	chr17:56736044..56736561-chr6:58778407..58779097,2	MCF-7	breast:
35	chr12:38031911..38033432-chr6:58776341..58779018,2	MCF-7	breast:
36	chr20:52238301..52240090-chr6:58777406..58779226,2	MCF-7	breast:
37	chr5:157496471..157496971-chr6:58776705..58777406,2	MCF-7	breast:
38	chr1:117112641..117113268-chr6:58775753..58776519,2	MCF-7	breast:
39	chr6:58776858..58779077-chr6:61908295..61909815,2	MCF-7	breast:
40	chr21:35272607..35275458-chr6:58776178..58778758,2	MCF-7	breast:
41	chr20:52560026..52560620-chr6:58777219..58777738,2	MCF-7	breast:
42	chr16:85495639..85498852-chr6:58775657..58778770,3	MCF-7	breast:
43	chr12:6493660..6495635-chr6:58777646..58779181,2	MCF-7	breast:
44	chr6:58776797..58778439-chr9:136323811..136326318,2	MCF-7	breast:
45	chr6:58777712..58778738-chr6:61909295..61909815,6	MCF-7	breast:
46	chr1:216349276..216351630-chr6:58776732..58778763,2	MCF-7	breast:
47	chr3:195577616..195578367-chr6:58777226..58778078,2	MCF-7	breast:
48	chr10:90750069..90750688-chr6:58777473..58778220,2	Hela-S3	cervix:
49	chr17:57930610..57932922-chr6:58777438..58780644,3	MCF-7	breast:
50	chr12:38032931..38033431-chr6:58776879..58777388,2	MCF-7	breast:

No data

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

Extended variants
information (count: 2208 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2208 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76280423	chr6:58773927-58773928	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
2	rs540012021	chr6:58773930-58773931	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs60855878	chr6:58773931-58773932	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs76124259	chr6:58773936-58773937	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs74425864	chr6:58773937-58773938	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs57021044	chr6:58773938-58773939	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs62412775	chr6:58773939-58773940	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs78261376	chr6:58773941-58773942	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs573510525	chr6:58773945-58773946	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs74195209	chr6:58773947-58773948	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs79443241	chr6:58773952-58773953	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs74217648	chr6:58773953-58773954	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs534263668	chr6:58773957-58773958	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs555627502	chr6:58773961-58773962	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs386701814	chr6:58773968-58773969	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs77262952	chr6:58773969-58773970	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs75277485	chr6:58773971-58773972	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs77799742	chr6:58773972-58773973	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs76660031	chr6:58773980-58773981	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs573965851	chr6:58773981-58773982	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs76084682	chr6:58773982-58773983	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs544287421	chr6:58773988-58773989	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs79156413	chr6:58773990-58773991	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs532918376	chr6:58773994-58773995	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs201786955	chr6:58773995-58773996	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs575468833	chr6:58773996-58773997	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs78197829	chr6:58773998-58773999	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs545727754	chr6:58773999-58774000	ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs76682319	chr6:58774002-58774003	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs552921986	chr6:58774004-58774005	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs566216843	chr6:58774005-58774006	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs546283793	chr6:58774006-58774007	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs112749178	chr6:58774007-58774008	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs113004069	chr6:58774009-58774010	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs76377972	chr6:58774010-58774011	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs561638911	chr6:58774013-58774014	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs528834503	chr6:58774014-58774015	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs386701815	chr6:58774024-58774025	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs74204040	chr6:58774026-58774027	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs550328577	chr6:58774039-58774040	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs569500793	chr6:58774040-58774041	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs540119951	chr6:58774041-58774042	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs77790960	chr6:58774044-58774045	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs552129928	chr6:58774046-58774047	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs567066837	chr6:58774051-58774052	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs534435327	chr6:58774054-58774055	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs555788033	chr6:58774055-58774056	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs548477717	chr6:58774056-58774057	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs538208695	chr6:58774062-58774063	ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs75780746	chr6:58774066-58774067	ZNF genes & repeats Bivalent Enhancer Weak transcription	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:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:58773400-58774000	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
2	chr6:58773400-58774000	Flanking Bivalent TSS/Enh	Hela-S3	cervix
3	chr6:58773400-58774800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr6:58773400-58774800	ZNF genes & repeats	Brain Hippocampus Middle	brain
5	chr6:58773400-58774800	ZNF genes & repeats	Colon Smooth Muscle	Colon
6	chr6:58773400-58774800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
7	chr6:58773400-58774800	ZNF genes & repeats	Fetal Lung	lung
8	chr6:58773400-58774800	ZNF genes & repeats	Rectal Smooth Muscle	rectum
9	chr6:58773400-58774800	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
10	chr6:58773400-58774800	ZNF genes & repeats	Stomach Smooth Muscle	stomach
11	chr6:58773400-58774800	ZNF genes & repeats	GM12878-XiMat	blood
12	chr6:58773400-58774800	ZNF genes & repeats	HUVEC	blood vessel
13	chr6:58773400-58775000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
14	chr6:58773400-58775000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr6:58773400-58775000	ZNF genes & repeats	Brain Anterior Caudate	brain
16	chr6:58773400-58775000	ZNF genes & repeats	Brain Cingulate Gyrus	brain
17	chr6:58773400-58775000	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
18	chr6:58773400-58775000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
19	chr6:58773400-58775000	ZNF genes & repeats	Dnd41	blood
20	chr6:58773400-58775200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr6:58773400-58775200	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr6:58773400-58775200	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
23	chr6:58773400-58775400	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
24	chr6:58773400-58775400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
25	chr6:58773400-58775600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
26	chr6:58773400-58775600	ZNF genes & repeats	Liver	Liver
27	chr6:58773400-58775800	ZNF genes & repeats	HMEC	breast
28	chr6:58773400-58776000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr6:58773400-58776000	ZNF genes & repeats	NH-A	brain
30	chr6:58773400-58776200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr6:58773400-58776200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr6:58773400-58776400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr6:58773400-58776400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
34	chr6:58773400-58776600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
35	chr6:58773400-58776600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
36	chr6:58773400-58776600	ZNF genes & repeats	Gastric	stomach
37	chr6:58773400-58776600	ZNF genes & repeats	Small Intestine	intestine
38	chr6:58773400-58779400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
39	chr6:58773400-58779400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr6:58773400-58779400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr6:58773400-58779400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
42	chr6:58773400-58779400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
43	chr6:58773400-58779400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
44	chr6:58773400-58779400	ZNF genes & repeats	Adipose Nuclei	Adipose
45	chr6:58773400-58779400	ZNF genes & repeats	Fetal Stomach	stomach
46	chr6:58773400-58779400	ZNF genes & repeats	Left Ventricle	heart
47	chr6:58773600-58774000	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr6:58773600-58774000	Flanking Bivalent TSS/Enh	Primary T helper naive cells from peripheral blood	blood
49	chr6:58773600-58774000	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
50	chr6:58773600-58774000	Flanking Bivalent TSS/Enh	Primary T killer naive cells fromperipheralblood	blood

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