Variant report

Variant	nsv516456
Chromosome Location	chr6:44282316-44298309
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:17)
CpG islands
(count:61)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:17 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr6:44284280-44284430	GM12878	blood:	n/a	n/a
2	CTCF	chr6:44282640-44282790	NHLF	lung:	n/a	n/a
3	FOXA2	chr6:44296304-44296682	A549	lung:	n/a	n/a
4	JUN	chr6:44290716-44290719	K562	blood:	n/a	n/a
5	JUND	chr6:44295987-44296119	H1-hESC	embryonic stem cell:	n/a	n/a
6	MAFK	chr6:44285920-44286167	HepG2	liver:	n/a	n/a
7	NR2F2	chr6:44284809-44285123	K562	blood:	n/a	n/a
8	NR2F2	chr6:44284803-44285203	K562	blood:	n/a	n/a
9	NR2F2	chr6:44296265-44296792	K562	blood:	n/a	n/a
10	POLR2A	chr6:44289040-44289106	MCF-7	breast:	n/a	n/a
11	POLR2A	chr6:44297494-44298070	H1-neurons	neurons:	n/a	n/a
12	POLR2A	chr6:44297584-44297984	H1-neurons	neurons:	n/a	n/a
13	POLR2A	chr6:44296153-44296185	H1-hESC	embryonic stem cell:	n/a	n/a
14	SETDB1	chr6:44288322-44288917	U2OS	brain:	n/a	n/a
15	SPI1	chr6:44284207-44284662	HL-60	blood:	n/a	n/a
16	USF1	chr6:44297306-44297609	K562	blood:	n/a	n/a
17	USF2	chr6:44297395-44297584	Hela-S3	cervix:	n/a	chr6:44297464-44297475

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:44295389-44295439	ovcar-3	ovarian:	n/a
2	chr6:44295389-44295439	NHBE	bronchial:	n/a
3	chr6:44295389-44295439	AoSMC	blood vessel:	n/a
4	chr6:44295389-44295439	H1-hESC	embryonic stem cell:	embryo
5	chr6:44295389-44295439	NH-A	brain:	n/a
6	chr6:44295389-44295439	HMEC	breast:	n/a
7	chr6:44295389-44295439	GM06990	blood:	n/a
8	chr6:44295389-44295439	A549	lung:	n/a
9	chr6:44295389-44295439	PFSK-1	brain:	n/a
10	chr6:44295389-44295439	HCPEpiC	choroid plexus:	n/a
11	chr6:44295389-44295439	GM12891	blood:	n/a
12	chr6:44295389-44295439	Jurkat	blood:	n/a
13	chr6:44295389-44295439	HEEpiC	esophagus:	n/a
14	chr6:44295389-44295439	NT2-D1	testis:	n/a
15	chr6:44295389-44295439	NHDF-neo	bronchial:	n/a
16	chr6:44295389-44295439	HCT-116	colon:	n/a
17	chr6:44295389-44295439	HUVEC	blood vessel:	n/a
18	chr6:44295389-44295439	SKMC	muscle:	n/a
19	chr6:44295389-44295439	AG09309	skin:	n/a
20	chr6:44295389-44295439	CMK	blood:	n/a
21	chr6:44295389-44295439	SK-N-SH	brain:	n/a
22	chr6:44295389-44295439	HepG2	liver:	n/a
23	chr6:44295389-44295439	AG10803	skin:	n/a
24	chr6:44295389-44295439	MCF-7	breast:	n/a
25	chr6:44295389-44295439	GM19239	blood:	n/a
26	chr6:44295389-44295439	LNCaP	prostate:	n/a
27	chr6:44295389-44295439	Hepatocyte	liver:	n/a
28	chr6:44295389-44295439	SAEC	small airway:	n/a
29	chr6:44295389-44295439	K562	blood:	n/a
30	chr6:44295389-44295439	HPAEpiC	pulmonary alveolar:	n/a
31	chr6:44295389-44295439	HRPEpiC	eye:	n/a
32	chr6:44295389-44295439	IMR90	lung:	fetal
33	chr6:44295389-44295439	Caco-2	colon:	n/a
34	chr6:44295389-44295439	T-47D	breast:	n/a
35	chr6:44295389-44295439	HL-60	blood:	n/a
36	chr6:44295389-44295439	RPTEC	kidney:	n/a
37	chr6:44295389-44295439	AG09319	gingival:	n/a
38	chr6:44295389-44295439	AG04449	skin:	fetal
39	chr6:44295389-44295439	BJ	skin:	n/a
40	chr6:44295389-44295439	MCF10A-Er-Src	breast:	n/a
41	chr6:44295389-44295439	PANC-1	pancreas:	n/a
42	chr6:44295389-44295439	U87	brain:	n/a
43	chr6:44295389-44295439	SK-N-MC	brain:	n/a
44	chr6:44295389-44295439	ProgFib	skin:	n/a
45	chr6:44295389-44295439	HRE	kidney:	n/a
46	chr6:44295389-44295439	GM12878	blood:	n/a
47	chr6:44295389-44295439	ECC-1	luminal epithelium:	n/a
48	chr6:44295389-44295439	SK-N-SH_RA	brain:	n/a
49	chr6:44295389-44295439	Hela-S3	cervix:	n/a
50	chr6:44295389-44295439	BE2_C	brain:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:44272619..44273140-chr6:44281766..44282700,2	K562	blood:
2	chr6:44290406..44293174-chr6:44296461..44299347,2	MCF-7	breast:
3	chr6:44297568..44299730-chr6:44300714..44302349,2	K562	blood:
4	chr6:44281326..44282860-chr6:44296235..44298156,2	K562	blood:
5	chr6:44213575..44218708-chr6:44278177..44283526,11	K562	blood:
6	chr6:44214113..44217135-chr6:44297677..44301069,3	K562	blood:
7	chr6:44292209..44295193-chr6:44309747..44312725,2	K562	blood:
8	chr6:44295218..44297676-chr6:44304954..44307920,2	K562	blood:
9	chr6:44281673..44282583-chr6:102995671..102996294,2	MCF-7	breast:
10	chr6:44279673..44281499-chr6:44291356..44293516,2	K562	blood:
11	chr6:44279978..44282464-chr6:44309513..44313447,3	K562	blood:
12	chr6:44279704..44282033-chr6:44282921..44285489,2	MCF-7	breast:
13	chr6:44213056..44218708-chr6:44277561..44284910,14	K562	blood:
14	chr6:44279670..44282519-chr6:44285796..44288892,3	MCF-7	breast:
15	chr6:44297560..44299730-chr6:44300849..44303984,3	K562	blood:
16	chr6:44281326..44282860-chr6:44296235..44298156,2	K562	blood:
17	chr6:44224383..44226876-chr6:44283913..44286827,2	MCF-7	breast:
18	chr6:44290406..44293174-chr6:44296461..44299347,2	MCF-7	breast:
19	chr6:44279584..44282464-chr6:44309477..44312125,3	K562	blood:
20	chr6:44234643..44237474-chr6:44296098..44297940,2	MCF-7	breast:
21	chr6:44223815..44226053-chr6:44279566..44282424,2	MCF-7	breast:
22	chr6:44279514..44281028-chr6:44297693..44300228,2	K562	blood:
23	chr6:44273300..44278087-chr6:44284295..44289273,5	MCF-7	breast:
24	chr6:44258945..44261017-chr6:44295322..44296917,2	MCF-7	breast:

No data

Variant related genes	Relation type
AARS2	TF binding region
AARS2	CpG island
ENSG00000249481	chromatin interactions
ENSG00000096384	chromatin interactions
ENSG00000157593	chromatin interactions
ENSG00000124608	chromatin interactions

Extended variants
information (count: 537 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:537 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4714776	chr6:44282316-44282317	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531071621	chr6:44282362-44282363	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs150597336	chr6:44282373-44282374	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs192543167	chr6:44282390-44282391	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs528653102	chr6:44282411-44282412	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs546827281	chr6:44282412-44282413	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs114586146	chr6:44282420-44282421	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs116518953	chr6:44282429-44282430	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs551057423	chr6:44282443-44282444	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs534293754	chr6:44282521-44282522	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs536693046	chr6:44282530-44282531	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs547811693	chr6:44282587-44282588	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs115991684	chr6:44282592-44282593	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs7763188	chr6:44282608-44282609	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs139610306	chr6:44282619-44282620	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs113231093	chr6:44282635-44282636	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs578118369	chr6:44282670-44282671	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs183461815	chr6:44282712-44282713	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs11398227	chr6:44282765-44282766	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs75304317	chr6:44282775-44282776	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs377728274	chr6:44282776-44282777	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs557027422	chr6:44282780-44282781	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs188305921	chr6:44282781-44282782	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs149724549	chr6:44282815-44282816	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs374074586	chr6:44282824-44282825	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs561613052	chr6:44282837-44282838	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs60453984	chr6:44282897-44282898	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs540400929	chr6:44282918-44282919	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs565154750	chr6:44282936-44282937	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs115506314	chr6:44282947-44282948	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs551452008	chr6:44283067-44283068	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs569687897	chr6:44283075-44283076	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs72864308	chr6:44283136-44283137	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs72864312	chr6:44283190-44283191	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs56303746	chr6:44283201-44283202	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs76208835	chr6:44283230-44283231	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs79602059	chr6:44283265-44283266	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs147394585	chr6:44283266-44283267	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs375570539	chr6:44283289-44283290	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs557531298	chr6:44283316-44283317	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs577314158	chr6:44283322-44283323	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs538505541	chr6:44283384-44283385	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs557417835	chr6:44283399-44283400	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs369753504	chr6:44283517-44283518	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs193180988	chr6:44283541-44283542	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs536629904	chr6:44283598-44283599	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs116614188	chr6:44283607-44283608	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs184403155	chr6:44283633-44283634	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs540536381	chr6:44283645-44283646	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs565280672	chr6:44283652-44283653	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Urothelial carcinoma	21177765	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
Cancer	20164920	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44281200-44283200	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr6:44281200-44283200	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr6:44281400-44283200	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr6:44281400-44283400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr6:44281600-44283600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr6:44283200-44283800	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr6:44283200-44284200	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr6:44283200-44285000	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr6:44283400-44283800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr6:44283600-44283800	Bivalent Enhancer	HSMMtube	muscle
11	chr6:44283600-44285400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr6:44284200-44284400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
13	chr6:44284200-44284600	Bivalent Enhancer	Placenta	Placenta
14	chr6:44285200-44285600	Bivalent Enhancer	HepG2	liver
15	chr6:44287000-44287200	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
16	chr6:44288000-44289800	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr6:44290400-44292800	Weak transcription	Right Atrium	heart
18	chr6:44292800-44294200	Strong transcription	Right Atrium	heart
19	chr6:44293200-44296200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr6:44293400-44293600	Enhancers	H9 Cell Line	embryonic stem cell
21	chr6:44293600-44293800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr6:44293800-44294800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr6:44294200-44297000	Weak transcription	Right Atrium	heart
24	chr6:44294400-44294600	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr6:44294400-44295800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr6:44294600-44295200	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr6:44294600-44295600	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr6:44294600-44296000	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr6:44294600-44296400	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr6:44294800-44297400	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr6:44295000-44295600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr6:44295000-44296000	Enhancers	H1 Cell Line	embryonic stem cell
33	chr6:44295000-44296200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr6:44295000-44296200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr6:44295000-44296800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr6:44295200-44295600	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr6:44295200-44296000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr6:44295200-44296200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:44295200-44296200	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr6:44295400-44295800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr6:44295400-44295800	Enhancers	H9 Cell Line	embryonic stem cell
42	chr6:44295600-44295800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
43	chr6:44295600-44295800	Bivalent Enhancer	Fetal Intestine Small	intestine
44	chr6:44295600-44296200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr6:44295600-44296200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr6:44295800-44296400	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr6:44295800-44300000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr6:44296000-44296200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
49	chr6:44296200-44300200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr6:44296200-44303600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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