Variant report

Variant	nsv960118
Chromosome Location	chr17:45501749-45503835
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:62)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:62 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr17:45503813-45503939	Spleen_OC	spleen:	n/a	n/a
2	EBF1	chr17:45503258-45503545	GM12878	blood:	n/a	n/a
3	POLR2A	chr17:45501845-45502133	H1-hESC	embryonic stem cell:	n/a	n/a
4	POLR2A	chr17:45502453-45503935	GM12878	blood:	n/a	n/a
5	POLR2A	chr17:45502659-45502993	Hela-S3	cervix:	n/a	n/a
6	POLR2A	chr17:45502471-45502987	GM12891	blood:	n/a	n/a
7	POLR2A	chr17:45503358-45503839	Hela-S3	cervix:	n/a	n/a
8	POLR2A	chr17:45502405-45503177	H1-hESC	embryonic stem cell:	n/a	n/a
9	POLR2A	chr17:45502652-45503062	GM12891	blood:	n/a	n/a
10	POLR2A	chr17:45502643-45502688	K562	blood:	n/a	n/a
11	POLR2A	chr17:45503153-45503850	GM12892	blood:	n/a	n/a
12	POLR2A	chr17:45503325-45503696	MCF-7	breast:	n/a	n/a
13	POLR2A	chr17:45501854-45502234	GM12891	blood:	n/a	n/a
14	POLR2A	chr17:45502175-45502223	MCF-7	breast:	n/a	n/a
15	POLR2A	chr17:45502634-45502893	HepG2	liver:	n/a	n/a
16	POLR2A	chr17:45502555-45503754	GM12891	blood:	n/a	n/a
17	POLR2A	chr17:45503087-45503153	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr17:45503717-45503743	MCF-7	breast:	n/a	n/a
19	POLR2A	chr17:45502685-45502854	GM12878	blood:	n/a	n/a
20	POLR2A	chr17:45502578-45503006	GM12892	blood:	n/a	n/a
21	POLR2A	chr17:45501719-45502285	GM12878	blood:	n/a	n/a
22	POLR2A	chr17:45501720-45502190	GM12892	blood:	n/a	n/a
23	POLR2A	chr17:45502947-45503019	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr17:45503497-45503583	GM12878	blood:	n/a	n/a
25	POLR2A	chr17:45503348-45503512	Hela-S3	cervix:	n/a	n/a
26	POLR2A	chr17:45501915-45502042	GM12878	blood:	n/a	n/a
27	POLR2A	chr17:45503745-45503784	MCF-7	breast:	n/a	n/a
28	POLR2A	chr17:45503064-45503075	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr17:45503311-45503478	GM12878	blood:	n/a	n/a
30	POLR2A	chr17:45501346-45502330	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr17:45502108-45502247	GM12891	blood:	n/a	n/a
32	POLR2A	chr17:45502438-45503925	GM12892	blood:	n/a	n/a
33	POLR2A	chr17:45503150-45503877	GM12891	blood:	n/a	n/a
34	POLR2A	chr17:45502537-45503017	GM12892	blood:	n/a	n/a
35	POLR2A	chr17:45502184-45502215	K562	blood:	n/a	n/a
36	POLR2A	chr17:45501753-45502263	GM12891	blood:	n/a	n/a
37	POLR2A	chr17:45502010-45502077	K562	blood:	n/a	n/a
38	POLR2A	chr17:45502652-45502921	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr17:45503357-45503592	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr17:45502738-45502776	K562	blood:	n/a	n/a
41	POLR2A	chr17:45502573-45503928	GM12892	blood:	n/a	n/a
42	POLR2A	chr17:45501842-45502059	GM12891	blood:	n/a	n/a
43	POLR2A	chr17:45502735-45502866	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr17:45501847-45502075	GM12878	blood:	n/a	n/a
45	POLR2A	chr17:45503113-45503801	GM12878	blood:	n/a	n/a
46	POLR2A	chr17:45502655-45503039	GM12878	blood:	n/a	n/a
47	POLR2A	chr17:45502533-45503048	MCF-7	breast:	n/a	n/a
48	POLR2A	chr17:45503268-45503511	GM12891	blood:	n/a	n/a
49	POLR2A	chr17:45503503-45503831	K562	blood:	n/a	n/a
50	POLR2A	chr17:45501774-45502157	GM12892	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45502151-45502201	HCF	heart:	n/a
2	chr17:45502151-45502201	HNPCEpiC	eye:	n/a
3	chr17:45502151-45502201	Caco-2	colon:	n/a
4	chr17:45502151-45502201	HIPEpiC	eye:	n/a
5	chr17:45502151-45502201	HAEpiC	amniotic membrane:	n/a
6	chr17:45502151-45502201	BJ	skin:	n/a
7	chr17:45502151-45502201	SK-N-MC	brain:	n/a
8	chr17:45502151-45502201	NT2-D1	testis:	n/a
9	chr17:45502151-45502201	SAEC	small airway:	n/a
10	chr17:45502151-45502201	MCF-7	breast:	n/a
11	chr17:45502151-45502201	AG10803	skin:	n/a
12	chr17:45502151-45502201	ovcar-3	ovarian:	n/a
13	chr17:45502151-45502201	HUVEC	blood vessel:	n/a
14	chr17:45502151-45502201	AG09319	gingival:	n/a
15	chr17:45502151-45502201	Jurkat	blood:	n/a
16	chr17:45502151-45502201	HepG2	liver:	n/a
17	chr17:45502151-45502201	IMR90	lung:	fetal
18	chr17:45502151-45502201	SK-N-SH_RA	brain:	n/a
19	chr17:45502151-45502201	MCF10A-Er-Src	breast:	n/a
20	chr17:45502151-45502201	HRCEpiC	kidney:	n/a
21	chr17:45502151-45502201	AG09309	skin:	n/a
22	chr17:45502151-45502201	HEEpiC	esophagus:	n/a
23	chr17:45502151-45502201	A549	lung:	n/a
24	chr17:45502151-45502201	HL-60	blood:	n/a
25	chr17:45502151-45502201	HCT-116	colon:	n/a
26	chr17:45502151-45502201	LNCaP	prostate:	n/a
27	chr17:45502151-45502201	HCM	heart:	n/a
28	chr17:45502151-45502201	HRPEpiC	eye:	n/a
29	chr17:45502151-45502201	HCPEpiC	choroid plexus:	n/a
30	chr17:45502151-45502201	ECC-1	luminal epithelium:	n/a
31	chr17:45502151-45502201	CMK	blood:	n/a
32	chr17:45502151-45502201	PrEC	prostate:	n/a
33	chr17:45502151-45502201	NHBE	bronchial:	n/a
34	chr17:45502151-45502201	RPTEC	kidney:	n/a
35	chr17:45502151-45502201	HEK293	kidney:	embryo
36	chr17:45502151-45502201	GM19239	blood:	n/a
37	chr17:45502151-45502201	U87	brain:	n/a
38	chr17:45502151-45502201	T-47D	breast:	n/a
39	chr17:45502151-45502201	Hela-S3	cervix:	n/a
40	chr17:45502151-45502201	K562	blood:	n/a
41	chr17:45502151-45502201	NB4	blood:	n/a
42	chr17:45502151-45502201	H1-hESC	embryonic stem cell:	embryo
43	chr17:45502151-45502201	SKMC	muscle:	n/a
44	chr17:45502151-45502201	HMEC	breast:	n/a
45	chr17:45502151-45502201	GM12891	blood:	n/a
46	chr17:45502151-45502201	ProgFib	skin:	n/a
47	chr17:45502151-45502201	Hepatocyte	liver:	n/a
48	chr17:45502151-45502201	GM12892	blood:	n/a
49	chr17:45502151-45502201	AG04450	lung:	fetal
50	chr17:45502151-45502201	NHDF-neo	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:45499733..45501782-chr17:45502052..45504438,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000253347	TF binding region
ENSG00000253347	CpG island
ENSG00000253347	chromatin interactions

Extended variants
information (count: 73 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:73 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541108536	chr17:45501805-45501806	Bivalent/Poised TSS Weak transcription Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs9909843	chr17:45501809-45501810	Bivalent/Poised TSS Weak transcription Strong transcription Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs184158651	chr17:45501812-45501813	Bivalent/Poised TSS Weak transcription Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs550072542	chr17:45501844-45501845	Bivalent/Poised TSS Weak transcription Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs112248488	chr17:45501859-45501860	Bivalent/Poised TSS Weak transcription Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs79257620	chr17:45501862-45501863	Bivalent/Poised TSS Weak transcription Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs139250546	chr17:45501868-45501869	Bivalent/Poised TSS Weak transcription Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs188836772	chr17:45501900-45501901	Bivalent/Poised TSS Weak transcription Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs375400790	chr17:45501960-45501961	Bivalent/Poised TSS Weak transcription Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs3826536	chr17:45501967-45501968	Bivalent/Poised TSS Weak transcription Strong transcription Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs138264090	chr17:45502026-45502027	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs112570832	chr17:45502054-45502055	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs547117381	chr17:45502081-45502082	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs9908049	chr17:45502096-45502097	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs376447789	chr17:45502164-45502165	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs113115744	chr17:45502165-45502166	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs537019797	chr17:45502169-45502170	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs557633985	chr17:45502194-45502195	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs548271723	chr17:45502240-45502241	Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs191820656	chr17:45502330-45502331	Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs184267804	chr17:45502342-45502343	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs553633722	chr17:45502343-45502344	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs189227749	chr17:45502373-45502374	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs539754840	chr17:45502434-45502435	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs111660881	chr17:45502465-45502466	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs371985623	chr17:45502491-45502492	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs576479600	chr17:45502494-45502495	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs62076507	chr17:45502537-45502538	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs543010667	chr17:45502544-45502545	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs553069410	chr17:45502545-45502546	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs563286025	chr17:45502559-45502560	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs532319799	chr17:45502576-45502577	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs552031133	chr17:45502606-45502607	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs559156391	chr17:45502607-45502608	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs528235567	chr17:45502615-45502616	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs548683917	chr17:45502649-45502650	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs568412505	chr17:45502778-45502779	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs185661976	chr17:45502792-45502793	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs188923876	chr17:45502808-45502809	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs570840986	chr17:45502839-45502840	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs143984402	chr17:45502851-45502852	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs181660677	chr17:45502866-45502867	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs573500900	chr17:45502914-45502915	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs185893373	chr17:45502921-45502922	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs554660592	chr17:45503016-45503017	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs146410948	chr17:45503028-45503029	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs541478272	chr17:45503054-45503055	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs140804767	chr17:45503121-45503122	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs189913829	chr17:45503147-45503148	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs78994662	chr17:45503176-45503177	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:117)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	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
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45490800-45502400	Weak transcription	HepG2	liver
2	chr17:45500400-45501800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
3	chr17:45500400-45501800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
4	chr17:45500400-45501800	Active TSS	Brain Angular Gyrus	brain
5	chr17:45500400-45501800	Active TSS	Rectal Mucosa Donor 29	rectum
6	chr17:45500400-45502000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
7	chr17:45500400-45502000	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr17:45500600-45501800	Active TSS	Duodenum Mucosa	Duodenum
9	chr17:45500600-45501800	Active TSS	Rectal Smooth Muscle	rectum
10	chr17:45500600-45501800	Active TSS	Osteobl	bone
11	chr17:45500600-45502000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
12	chr17:45500600-45502000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
13	chr17:45500600-45502000	Active TSS	Fetal Intestine Large	intestine
14	chr17:45500600-45502000	Active TSS	Fetal Intestine Small	intestine
15	chr17:45500600-45502000	Active TSS	Rectal Mucosa Donor 31	rectum
16	chr17:45500600-45502200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
17	chr17:45500600-45511200	Weak transcription	K562	blood
18	chr17:45500800-45501800	Active TSS	H9 Cell Line	embryonic stem cell
19	chr17:45500800-45501800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr17:45500800-45501800	Active TSS	Breast Myoepithelial Primary Cells	Breast
21	chr17:45500800-45501800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr17:45500800-45501800	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
23	chr17:45500800-45501800	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
24	chr17:45500800-45501800	Bivalent/Poised TSS	Fetal Stomach	stomach
25	chr17:45500800-45501800	Active TSS	NH-A	brain
26	chr17:45500800-45502000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
27	chr17:45500800-45502000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
28	chr17:45500800-45506800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr17:45501000-45501800	Enhancers	Primary B cells from cord blood	blood
30	chr17:45501000-45501800	Bivalent/Poised TSS	Fetal Brain Female	brain
31	chr17:45501000-45502000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr17:45501400-45501800	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
33	chr17:45501400-45501800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr17:45501400-45501800	Enhancers	Liver	Liver
35	chr17:45501400-45501800	Active TSS	Colonic Mucosa	Colon
36	chr17:45501400-45501800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr17:45501400-45501800	Active TSS	Placenta	Placenta
38	chr17:45501400-45502600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr17:45501400-45504800	Weak transcription	A549	lung
40	chr17:45501400-45514600	Weak transcription	Primary T cells from cord blood	blood
41	chr17:45501400-45554200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr17:45501400-45554400	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr17:45501600-45501800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr17:45501600-45501800	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr17:45501600-45501800	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr17:45501600-45501800	Active TSS	Cortex derived primary cultured neurospheres	brain
47	chr17:45501600-45501800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr17:45501600-45501800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr17:45501600-45501800	Active TSS	Duodenum Smooth Muscle	Duodenum
50	chr17:45501600-45501800	Flanking Active TSS	Gastric	stomach

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