Variant report

Variant	esv3380735
Chromosome Location	chr17:34246253-34271932
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:357)
CpG islands
(count:1159)
Chromatin interactive
region (count:9)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:34269673-34270090	K562	blood:	n/a	n/a
2	ARID3A	chr17:34257775-34258459	K562	blood:	n/a	n/a
3	ATF1	chr17:34269537-34270013	K562	blood:	n/a	n/a
4	ATF3	chr17:34263092-34263365	K562	blood:	n/a	n/a
5	ATF3	chr17:34257587-34258081	A549	lung:	n/a	n/a
6	ATF3	chr17:34257493-34258046	A549	lung:	n/a	n/a
7	BATF	chr17:34250677-34251014	GM12878	blood:	n/a	n/a
8	BATF	chr17:34250767-34250988	GM12878	blood:	n/a	n/a
9	BCL3	chr17:34257372-34258096	A549	lung:	n/a	n/a
10	BCLAF1	chr17:34257426-34257998	GM12878	blood:	n/a	n/a
11	BHLHE40	chr17:34269660-34269820	K562	blood:	n/a	n/a
12	BHLHE40	chr17:34257606-34257989	GM12878	blood:	n/a	n/a
13	BHLHE40	chr17:34257613-34258093	K562	blood:	n/a	n/a
14	CBX3	chr17:34257536-34258177	K562	blood:	n/a	n/a
15	CCNT2	chr17:34269655-34270067	K562	blood:	n/a	n/a
16	CEBPB	chr17:34263067-34263332	HepG2	liver:	n/a	chr17:34263182-34263193
17	CEBPB	chr17:34268976-34269176	HepG2	liver:	n/a	n/a
18	CEBPB	chr17:34263140-34263334	IMR90	lung:	n/a	chr17:34263182-34263193
19	CEBPB	chr17:34269121-34269127	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr17:34256289-34256435	K562	blood:	n/a	n/a
21	CEBPB	chr17:34263036-34263366	K562	blood:	n/a	chr17:34263182-34263193
22	CEBPB	chr17:34263124-34263343	A549	lung:	n/a	chr17:34263182-34263193
23	CEBPB	chr17:34263085-34263369	K562	blood:	n/a	chr17:34263182-34263193
24	CEBPB	chr17:34258460-34258465	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPD	chr17:34269566-34270107	K562	blood:	n/a	n/a
26	CEBPD	chr17:34269471-34270192	K562	blood:	n/a	n/a
27	CHD1	chr17:34257359-34257667	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr17:34257548-34258043	GM12878	blood:	n/a	n/a
29	CHD2	chr17:34257692-34258069	K562	blood:	n/a	n/a
30	CHD2	chr17:34257596-34257993	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr17:34257521-34257943	A549	lung:	n/a	n/a
32	CTCF	chr17:34255208-34255230	GM10266	blood:	n/a	n/a
33	CTCF	chr17:34257733-34257802	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr17:34262632-34262652	GM13976	blood:	n/a	n/a
35	CTCF	chr17:34271899-34271933	GM12878	blood:	n/a	n/a
36	CTCF	chr17:34271866-34271895	GM13977	blood:	n/a	n/a
37	CTCF	chr17:34271823-34271943	GM10266	blood:	n/a	n/a
38	CTCF	chr17:34257700-34257850	GM12873	blood:	n/a	n/a
39	CTCF	chr17:34257360-34257510	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr17:34271885-34271896	GM12878	blood:	n/a	n/a
41	CTCF	chr17:34271817-34271944	K562	blood:	n/a	n/a
42	CTCF	chr17:34266500-34266650	Caco-2	colon:	n/a	n/a
43	CTCF	chr17:34271796-34271945	K562	blood:	n/a	n/a
44	CTCF	chr17:34271880-34272030	GM12875	blood:	n/a	n/a
45	E2F4	chr17:34257473-34258524	MCF10A-Er-Src	breast:	n/a	chr17:34257776-34257785
46	E2F4	chr17:34257561-34258005	K562	blood:	n/a	chr17:34257776-34257785
47	E2F4	chr17:34257565-34257987	Hela-S3	cervix:	n/a	chr17:34257776-34257785
48	E2F4	chr17:34252727-34252758	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr17:34259513-34259601	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr17:34257595-34258016	GM12878	blood:	n/a	chr17:34257776-34257785

(count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:34258202-34258252	HepG2	liver:	n/a
2	chr17:34257936-34257986	GM12892	blood:	n/a
3	chr17:34257726-34257776	Hepatocyte	liver:	n/a
4	chr17:34258076-34258126	AoSMC	blood vessel:	n/a
5	chr17:34255494-34255544	HL-60	blood:	n/a
6	chr17:34257936-34257986	HRE	kidney:	n/a
7	chr17:34257659-34257709	H1-hESC	embryonic stem cell:	embryo
8	chr17:34257435-34257485	HRPEpiC	eye:	n/a
9	chr17:34261810-34261860	AG09309	skin:	n/a
10	chr17:34267111-34267161	CMK	blood:	n/a
11	chr17:34257435-34257485	HNPCEpiC	eye:	n/a
12	chr17:34271125-34271175	ProgFib	skin:	n/a
13	chr17:34258076-34258126	MCF-7	breast:	n/a
14	chr17:34266290-34266340	PANC-1	pancreas:	n/a
15	chr17:34271125-34271175	HCPEpiC	choroid plexus:	n/a
16	chr17:34257435-34257485	Hela-S3	cervix:	n/a
17	chr17:34261789-34261839	PANC-1	pancreas:	n/a
18	chr17:34257936-34257986	HEEpiC	esophagus:	n/a
19	chr17:34257462-34257512	SK-N-MC	brain:	n/a
20	chr17:34258218-34258268	NH-A	brain:	n/a
21	chr17:34257462-34257512	HRE	kidney:	n/a
22	chr17:34257571-34257621	HPAEpiC	pulmonary alveolar:	n/a
23	chr17:34267111-34267161	HIPEpiC	eye:	n/a
24	chr17:34258076-34258126	GM12892	blood:	n/a
25	chr17:34271125-34271175	IMR90	lung:	fetal
26	chr17:34271125-34271175	AG09309	skin:	n/a
27	chr17:34258202-34258252	HPAEpiC	pulmonary alveolar:	n/a
28	chr17:34257764-34257814	IMR90	lung:	fetal
29	chr17:34258202-34258252	HNPCEpiC	eye:	n/a
30	chr17:34255494-34255544	NHBE	bronchial:	n/a
31	chr17:34267757-34267807	GM19239	blood:	n/a
32	chr17:34261789-34261839	PrEC	prostate:	n/a
33	chr17:34257659-34257709	NH-A	brain:	n/a
34	chr17:34257435-34257485	Hepatocyte	liver:	n/a
35	chr17:34271125-34271175	RPTEC	kidney:	n/a
36	chr17:34257001-34257051	HPAEpiC	pulmonary alveolar:	n/a
37	chr17:34271125-34271175	AoSMC	blood vessel:	n/a
38	chr17:34257435-34257485	SK-N-MC	brain:	n/a
39	chr17:34257001-34257051	SK-N-MC	brain:	n/a
40	chr17:34267111-34267161	AoSMC	blood vessel:	n/a
41	chr17:34257936-34257986	HNPCEpiC	eye:	n/a
42	chr17:34257462-34257512	HCM	heart:	n/a
43	chr17:34257764-34257814	GM12878	blood:	n/a
44	chr17:34257435-34257485	GM12892	blood:	n/a
45	chr17:34257659-34257709	LNCaP	prostate:	n/a
46	chr17:34266290-34266340	MCF-7	breast:	n/a
47	chr17:34255494-34255544	AG10803	skin:	n/a
48	chr17:34261810-34261860	HRE	kidney:	n/a
49	chr17:34257435-34257485	HEK293	kidney:	embryo
50	chr17:34257936-34257986	SK-N-SH_RA	brain:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:34257293..34261101-chr17:34262083..34265206,5	K562	blood:
2	chr17:34236497..34238510-chr17:34243558..34246809,3	K562	blood:
3	chr17:34244266..34246536-chr17:34253615..34255609,2	K562	blood:
4	chr17:34242717..34244891-chr17:34245039..34247861,2	K562	blood:
5	chr17:34257735..34259695-chr17:34260780..34264924,4	K562	blood:
6	chr17:34264862..34267825-chr17:34271764..34274325,3	K562	blood:
7	chr17:34250004..34251534-chr17:34256456..34258888,2	K562	blood:
8	chr17:34263107..34265585-chr4:113207766..113210422,2	MCF-7	breast:
9	chr17:34237936..34240091-chr17:34247001..34248563,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RDM1-2	chr17:34247191-34247276	NR_028000
2	lnc-RDM1-2	chr17:34252519-34252641	NR_027996
3	lnc-RDM1-2	chr17:34247191-34247276	NR_027996
4	lnc-RDM1-2	chr17:34249581-34249679	NR_028000
5	lnc-RDM1-2	chr17:34257636-34257780	NR_027996
6	lnc-RDM1-2	chr17:34252519-34252641	NR_028000
7	lnc-RDM1-2	chr17:34257080-34257303	NR_028000
8	lnc-RDM1-2	chr17:34249581-34249679	NR_027996

No data

Variant related genes	Relation type
LRRC37A9P	TF binding region
LYZL6	TF binding region
RDM1	TF binding region
LRRC37A9P	CpG island
LYZL6	CpG island
RDM1	CpG island
ENSG00000266999	chromatin interactions
ENSG00000266972	chromatin interactions
ENSG00000161572	chromatin interactions
ENSG00000187456	chromatin interactions

Extended variants
information (count: 1038 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114898584	chr17:34246258-34246259	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs572387290	chr17:34246307-34246308	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs541191100	chr17:34246310-34246311	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs187541770	chr17:34246320-34246321	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs78588723	chr17:34246371-34246372	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs72040262	chr17:34246372-34246373	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs192600022	chr17:34246374-34246375	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs9890583	chr17:34246393-34246394	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs139001027	chr17:34246488-34246489	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs531550383	chr17:34246531-34246532	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs80314171	chr17:34246542-34246543	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs562008400	chr17:34246614-34246615	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs527959889	chr17:34246632-34246633	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs115175143	chr17:34246645-34246646	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs143026514	chr17:34246670-34246671	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs78338352	chr17:34246680-34246681	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs549855580	chr17:34246681-34246682	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs569778253	chr17:34246711-34246712	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs535406787	chr17:34246737-34246738	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs555424727	chr17:34246756-34246757	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs2702949	chr17:34246757-34246758	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs534598364	chr17:34246765-34246766	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs558071779	chr17:34246768-34246769	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs370719279	chr17:34246803-34246804	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs567600010	chr17:34246810-34246811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs144693625	chr17:34246817-34246818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552736841	chr17:34246847-34246848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs2376287	chr17:34246869-34246870	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs183364780	chr17:34246874-34246875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs148581978	chr17:34246915-34246916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187663263	chr17:34246947-34246948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs56039715	chr17:34246979-34246980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs55691418	chr17:34247014-34247015	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs541360330	chr17:34247015-34247016	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184783774	chr17:34247038-34247039	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs533324768	chr17:34247079-34247080	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs577296634	chr17:34247096-34247097	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs546265173	chr17:34247131-34247132	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs189735938	chr17:34247140-34247141	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs374263417	chr17:34247167-34247168	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs201176535	chr17:34247171-34247172	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs200246131	chr17:34247174-34247175	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs372019272	chr17:34247192-34247193	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs202104033	chr17:34247202-34247203	Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs2526325	chr17:34247218-34247219	Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs192386068	chr17:34247222-34247223	Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs201025749	chr17:34247230-34247231	Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs375417161	chr17:34247232-34247233	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
49	rs138809711	chr17:34247239-34247240	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
50	rs149365928	chr17:34247244-34247245	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Melanoma	18172304	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cancer	20164919	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
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	17603634	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
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17157792	CNVD
Bladder cancer	19088036	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
Meningioma	19431122	CNVD
Neurocytoma	17123091	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Cervical cancer	21062161	CNVD
Colorectal cancer	22860045	CNVD
Ductal carcinoma	18381933	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16417655	CNVD
Renal cysts	20603712	CNVD
Epilepsy	21858020	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Autism	20587423	CNVD
Renal cysts	20587423	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Mayer-Rokitansky-Kuster-Hauser syndrome	19889212	CNVD
Endometrial cancer	23636398	CNVD
Urothelial cell carcinoma	18451213	CNVD
Gastric cancer	24379144	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	17850661	CNVD
Primary lung adenocarcinoma	16799635	CNVD
HIV/AIDS	18848619	CNVD
Rheumatoid arthritis	19220326	CNVD
Rheumatoid arthritis	18848619	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	18848619	CNVD
Type 1 diabetes	19220326	CNVD
HIV/AIDS	17330138	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Acute monocytic leukemia	16498392	CNVD
Breast cancer	20409316	CNVD
Myelodysplastic syndrome	18663149	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	19153074	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20932292	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Adrenocortical carcinoma	18281524	CNVD
Lung cancer	21569311	CNVD
Gastric cancer	21811585	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:539 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:34234600-34251200	Weak transcription	Fetal Thymus	thymus
2	chr17:34242600-34251400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr17:34243000-34249600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr17:34244600-34252200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr17:34244800-34256800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr17:34244800-34257000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr17:34245400-34250000	Weak transcription	Fetal Intestine Small	intestine
8	chr17:34245400-34255000	Weak transcription	Fetal Intestine Large	intestine
9	chr17:34245600-34246600	Weak transcription	K562	blood
10	chr17:34245600-34257200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr17:34245800-34247400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr17:34245800-34251400	Weak transcription	Primary T cells from cord blood	blood
13	chr17:34246000-34249600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr17:34246000-34251200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr17:34246000-34256800	Weak transcription	Primary hematopoietic stem cells	blood
16	chr17:34246000-34256800	Weak transcription	Thymus	Thymus
17	chr17:34246200-34249400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr17:34246600-34247000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr17:34246600-34247000	Enhancers	K562	blood
20	chr17:34247000-34247200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr17:34247000-34247400	Flanking Active TSS	K562	blood
22	chr17:34247200-34256800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr17:34247400-34248400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr17:34247400-34248600	Enhancers	K562	blood
25	chr17:34247400-34257000	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr17:34247600-34250600	Weak transcription	GM12878-XiMat	blood
27	chr17:34247600-34257000	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr17:34248200-34251000	Weak transcription	Primary B cells from cord blood	blood
29	chr17:34248200-34256200	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr17:34248200-34256800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr17:34248400-34250600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr17:34248600-34256600	Weak transcription	K562	blood
33	chr17:34249400-34250200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr17:34249600-34250200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
35	chr17:34249600-34251600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr17:34249800-34257000	Weak transcription	Fetal Muscle Leg	muscle
37	chr17:34250000-34252200	Strong transcription	Fetal Intestine Small	intestine
38	chr17:34250200-34256800	Weak transcription	A549	lung
39	chr17:34250200-34257000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr17:34250200-34257000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr17:34250600-34251800	Enhancers	Primary B cells from peripheral blood	blood
42	chr17:34250600-34251800	Enhancers	GM12878-XiMat	blood
43	chr17:34250600-34252000	Enhancers	Primary T cells fromperipheralblood	blood
44	chr17:34250600-34252000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr17:34250800-34251800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr17:34251000-34251800	Enhancers	Primary B cells from cord blood	blood
47	chr17:34251200-34251400	Enhancers	Fetal Thymus	thymus
48	chr17:34251200-34251600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr17:34251400-34251800	Enhancers	Primary T cells from cord blood	blood
50	chr17:34251400-34251800	Enhancers	Primary T helper naive cells from peripheral blood	blood

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