Variant report

Variant	nsv1028068
Chromosome Location	chr6:45169010-45246577
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:273)
CpG islands
(count:0)
Chromatin interactive
region (count:22)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:273 , 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	chr6:45232739-45233458	HepG2	liver:	n/a	chr6:45232952-45232968
2	ATF1	chr6:45177616-45177798	K562	blood:	n/a	n/a
3	ATF1	chr6:45190091-45190279	K562	blood:	n/a	n/a
4	BACH1	chr6:45180959-45180963	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr6:45210390-45210813	HCT-116	colon:	n/a	n/a
6	CBX3	chr6:45207452-45207700	K562	blood:	n/a	n/a
7	CBX3	chr6:45199417-45199794	K562	blood:	n/a	n/a
8	CBX3	chr6:45208754-45209051	K562	blood:	n/a	n/a
9	CBX3	chr6:45199449-45199702	K562	blood:	n/a	n/a
10	CBX3	chr6:45208754-45209148	K562	blood:	n/a	n/a
11	CEBPB	chr6:45184702-45184889	A549	lung:	n/a	n/a
12	CEBPB	chr6:45173462-45173620	K562	blood:	n/a	n/a
13	CEBPB	chr6:45210528-45210647	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr6:45233125-45233428	IMR90	lung:	n/a	chr6:45233290-45233301
15	CEBPB	chr6:45173401-45173601	K562	blood:	n/a	n/a
16	CEBPB	chr6:45200403-45200505	HepG2	liver:	n/a	n/a
17	CEBPB	chr6:45233172-45233354	HepG2	liver:	n/a	chr6:45233290-45233301
18	CEBPB	chr6:45233106-45233415	HepG2	liver:	n/a	chr6:45233290-45233301
19	CHD2	chr6:45238010-45238307	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr6:45238008-45238362	K562	blood:	n/a	n/a
21	CTCF	chr6:45193960-45194110	HPF	lung:	n/a	chr6:45194005-45194014
22	CTCF	chr6:45193920-45194070	BJ	skin:	n/a	chr6:45194005-45194014
23	CTCF	chr6:45193920-45194070	HCPEpiC	choroid plexus:	n/a	chr6:45194005-45194014
24	CTCF	chr6:45193920-45194070	K562	blood:	n/a	chr6:45194005-45194014
25	CTCF	chr6:45193980-45194130	NHDF-neo	bronchial:	n/a	chr6:45194005-45194014
26	CTCF	chr6:45206965-45207050	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr6:45193900-45194050	GM12873	blood:	n/a	chr6:45194005-45194014
28	CTCF	chr6:45193997-45194069	GM10248	blood:	n/a	chr6:45194005-45194014
29	CTCF	chr6:45193980-45194130	GM12865	blood:	n/a	chr6:45194005-45194014
30	CTCF	chr6:45193820-45193970	RPTEC	kidney:	n/a	n/a
31	CTCF	chr6:45193980-45194130	GM12874	blood:	n/a	chr6:45194005-45194014
32	CTCF	chr6:45193920-45194070	HRPEpiC	eye:	n/a	chr6:45194005-45194014
33	CTCF	chr6:45194005-45194057	LNCaP	prostate:	n/a	chr6:45194005-45194014
34	CTCF	chr6:45193940-45194090	MCF-7	breast:	n/a	chr6:45194005-45194014
35	CTCF	chr6:45193940-45194090	HMF	breast:	n/a	chr6:45194005-45194014
36	CTCF	chr6:45224860-45225010	GM12871	blood:	n/a	n/a
37	CTCF	chr6:45193960-45194110	HMF	breast:	n/a	chr6:45194005-45194014
38	CTCF	chr6:45193960-45194110	HPAF	blood vessel:	n/a	chr6:45194005-45194014
39	CTCF	chr6:45193990-45194048	GM12878	blood:	n/a	chr6:45194005-45194014
40	CTCF	chr6:45193940-45194090	HRPEpiC	eye:	n/a	chr6:45194005-45194014
41	CTCF	chr6:45184340-45184490	HMF	breast:	n/a	n/a
42	CTCF	chr6:45193880-45194030	HMEC	breast:	n/a	chr6:45194005-45194014
43	CTCF	chr6:45193880-45194030	AG09309	skin:	n/a	chr6:45194005-45194014
44	CTCF	chr6:45193960-45194110	NHDF-neo	bronchial:	n/a	chr6:45194005-45194014
45	CTCF	chr6:45182786-45182800	Lung_OC	lung:	n/a	n/a
46	CTCF	chr6:45193860-45194010	HepG2	liver:	n/a	n/a
47	CTCF	chr6:45228580-45228730	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr6:45201040-45201190	K562	blood:	n/a	n/a
49	CTCF	chr6:45193980-45194130	HCM	heart:	n/a	chr6:45194005-45194014
50	CTCF	chr6:45193840-45193990	RPTEC	kidney:	n/a	n/a

No data

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:45163170..45165177-chr6:45169368..45170904,2	K562	blood:
2	chr6:45235925..45238854-chr6:45344533..45347145,2	K562	blood:
3	chr6:45226327..45228586-chr6:45230289..45234245,4	K562	blood:
4	chr6:45172898..45174663-chr6:45183138..45184691,2	K562	blood:
5	chr6:45232941..45235847-chr6:45236328..45239058,2	MCF-7	breast:
6	chr15:98568515..98569332-chr6:45179144..45180022,2	MCF-7	breast:
7	chr6:45170143..45173003-chr6:45173758..45175670,2	MCF-7	breast:
8	chr6:45172898..45174663-chr6:45183138..45184691,2	K562	blood:
9	chr6:45169238..45172047-chr6:45343941..45345557,2	MCF-7	breast:
10	chr6:45170143..45173003-chr6:45173758..45175670,2	MCF-7	breast:
11	chr6:45200553..45203015-chr6:45211837..45214861,3	K562	blood:
12	chr6:45171517..45174411-chr6:45178235..45180217,2	K562	blood:
13	chr6:45200553..45203015-chr6:45211837..45214861,3	K562	blood:
14	chr6:45213921..45216260-chr6:45230809..45233624,3	K562	blood:
15	chr6:45213921..45216260-chr6:45230809..45233624,3	K562	blood:
16	chr6:45226327..45228586-chr6:45230289..45234245,4	K562	blood:
17	chr6:45220520..45222060-chr6:45226309..45228939,2	MCF-7	breast:
18	chr6:45171517..45174411-chr6:45178235..45180217,2	K562	blood:
19	chr6:45232941..45235847-chr6:45236328..45239058,2	MCF-7	breast:
20	chr20:59263227..59263735-chr6:45242300..45243068,2	MCF-7	breast:
21	chr6:45220520..45222060-chr6:45226309..45228939,2	MCF-7	breast:
22	chr6:45160972..45165246-chr6:45178939..45182549,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLIC5-2	chr6:45227825-45227890	ENSG00000230554.1
2	lnc-CLIC5-2	chr6:45227949-45228305	ENSG00000230554.1
3	lnc-CLIC5-3	chr6:45218692-45218873	NONHSAT112976

No data

Variant related genes	Relation type
MIR586	TF binding region
ENSG00000252477	chromatin interactions
ENSG00000196284	chromatin interactions

Extended variants
information (count: 2799 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2799 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200382718	chr6:45169031-45169032	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs138088243	chr6:45169056-45169057	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs570143995	chr6:45169111-45169112	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs577389433	chr6:45169131-45169132	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs6905396	chr6:45169165-45169166	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs549563071	chr6:45169172-45169173	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs149525800	chr6:45169193-45169194	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs147196588	chr6:45169201-45169202	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs553547366	chr6:45169205-45169206	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs115299492	chr6:45169222-45169223	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs370902051	chr6:45169251-45169252	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs180823577	chr6:45169299-45169300	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs539424477	chr6:45169329-45169330	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs184886639	chr6:45169417-45169418	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs189750135	chr6:45169424-45169425	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs543568503	chr6:45169448-45169449	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs555979670	chr6:45169458-45169459	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs79861159	chr6:45169467-45169468	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs140472250	chr6:45169511-45169512	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs560091293	chr6:45169533-45169534	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs181148930	chr6:45169534-45169535	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs376060782	chr6:45169561-45169562	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs4714842	chr6:45169614-45169615	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs370164224	chr6:45169666-45169667	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs563580210	chr6:45169667-45169668	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs531013301	chr6:45169668-45169669	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs186480673	chr6:45169820-45169821	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs563193697	chr6:45169928-45169929	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs191777104	chr6:45170022-45170023	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs144384183	chr6:45170045-45170046	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs547245123	chr6:45170062-45170063	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs147386971	chr6:45170067-45170068	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs551958946	chr6:45170089-45170090	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs1284955	chr6:45170121-45170122	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs1284956	chr6:45170151-45170152	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs527815107	chr6:45170154-45170155	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs569582932	chr6:45170182-45170183	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs183605595	chr6:45170196-45170197	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs555522248	chr6:45170259-45170260	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs574238091	chr6:45170276-45170277	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs148428967	chr6:45170301-45170302	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs187888284	chr6:45170320-45170321	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs578195011	chr6:45170325-45170326	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs554600831	chr6:45170326-45170327	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs73735312	chr6:45170335-45170336	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs563689766	chr6:45170346-45170347	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs183409533	chr6:45170375-45170376	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs542663931	chr6:45170384-45170385	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs561066195	chr6:45170388-45170389	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs142513395	chr6:45170389-45170390	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
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
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	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
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	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
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Ovarian cancer	20844748	CNVD
lymphocytic leukemia	21291569	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
Heart disease	21282601	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	16608533	CNVD

Chromatin state (count:242 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:45162000-45171800	Enhancers	Dnd41	blood
2	chr6:45168400-45169200	Enhancers	HepG2	liver
3	chr6:45168600-45169200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr6:45168800-45169800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr6:45169200-45169400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr6:45169200-45169400	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr6:45169200-45174400	Weak transcription	HepG2	liver
8	chr6:45170400-45170800	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr6:45171000-45171400	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr6:45171800-45173200	Weak transcription	Dnd41	blood
11	chr6:45173200-45175600	Enhancers	Dnd41	blood
12	chr6:45174400-45175800	Enhancers	HepG2	liver
13	chr6:45175000-45175200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr6:45175200-45175400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr6:45175400-45178000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr6:45175600-45178800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr6:45175800-45177400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
18	chr6:45176400-45177800	ZNF genes & repeats	Dnd41	blood
19	chr6:45176400-45178200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
20	chr6:45176600-45176800	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
21	chr6:45176800-45177600	Weak transcription	Fetal Thymus	thymus
22	chr6:45176800-45177800	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr6:45177000-45177200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr6:45177200-45177600	Weak transcription	Fetal Kidney	kidney
25	chr6:45177600-45178000	Enhancers	Fetal Thymus	thymus
26	chr6:45177800-45178400	Enhancers	Muscle Satellite Cultured Cells	--
27	chr6:45177800-45179000	Enhancers	Dnd41	blood
28	chr6:45178200-45182200	Weak transcription	Primary hematopoietic stem cells	blood
29	chr6:45179000-45180200	Weak transcription	Dnd41	blood
30	chr6:45179600-45179800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr6:45179800-45181000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr6:45179800-45182400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr6:45179800-45182600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr6:45180000-45182000	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr6:45180000-45182000	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr6:45180000-45182600	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr6:45180200-45180600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:45180200-45180600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr6:45180200-45181200	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr6:45180200-45181200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr6:45180200-45181400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr6:45180200-45182400	Enhancers	Dnd41	blood
43	chr6:45180200-45182800	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr6:45180400-45180800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr6:45180400-45181000	Enhancers	H1 Cell Line	embryonic stem cell
46	chr6:45180400-45181000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr6:45180400-45181400	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr6:45180600-45180800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr6:45180600-45181000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr6:45180600-45181200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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