Variant report

Variant	nsv960101
Chromosome Location	chr17:38594067-38597269
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr17:38597169-38597607	K562	blood:	n/a	n/a
2	CREB1	chr17:38597184-38597584	A549	lung:	n/a	n/a
3	CTCF	chr17:38597181-38597703	HCT-116	colon:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
4	CTCF	chr17:38595300-38595450	HPAF	blood vessel:	n/a	chr17:38595360-38595369
5	CTCF	chr17:38595300-38595450	GM12873	blood:	n/a	chr17:38595360-38595369
6	CTCF	chr17:38597210-38597609	IMR90	lung:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
7	CTCF	chr17:38597261-38597546	LNCaP	prostate:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
8	CTCF	chr17:38595280-38595430	SK-N-SH_RA	brain:	n/a	chr17:38595360-38595369
9	CTCF	chr17:38597259-38597555	GM12878	blood:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
10	CTCF	chr17:38595240-38595390	BE2_C	brain:	n/a	chr17:38595360-38595369
11	CTCF	chr17:38597259-38597566	GM12892	blood:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
12	CTCF	chr17:38597255-38597556	Medullo	brain:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
13	CTCF	chr17:38595280-38595430	BE2_C	brain:	n/a	chr17:38595360-38595369
14	CTCF	chr17:38597152-38597564	A549	lung:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
15	CTCF	chr17:38597147-38597576	MCF-7	breast:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
16	CTCF	chr17:38595300-38595450	HEK293	kidney:	n/a	chr17:38595360-38595369
17	CTCF	chr17:38597221-38597615	A549	lung:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
18	CTCF	chr17:38597208-38597605	GM12878	blood:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
19	CTCF	chr17:38595899-38596102	K562	blood:	n/a	n/a
20	CTCF	chr17:38595160-38595310	GM12873	blood:	n/a	n/a
21	CTCF	chr17:38597168-38597645	T-47D	breast:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
22	CTCF	chr17:38597008-38598019	A549	lung:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
23	CTCF	chr17:38597240-38597390	HAc	cerebellar:	n/a	n/a
24	CTCF	chr17:38597268-38597547	HUVEC	blood vessel:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
25	CTCF	chr17:38597198-38597566	H1-hESC	embryonic stem cell:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
26	CTCF	chr17:38595220-38595370	GM12867	blood:	n/a	chr17:38595360-38595369
27	CTCF	chr17:38597255-38597566	GM19240	blood:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
28	CTCF	chr17:38595260-38595410	WERI-Rb-1	eye:	n/a	chr17:38595360-38595369
29	CTCF	chr17:38595360-38595510	HBMEC	blood vessel:	n/a	chr17:38595360-38595369
30	CTCF	chr17:38597253-38597580	GM19238	blood:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
31	CTCF	chr17:38595134-38595147	GM10266	blood:	n/a	n/a
32	CTCF	chr17:38597267-38597560	MCF-7	breast:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
33	CTCF	chr17:38597268-38597555	MCF-7	breast:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
34	CTCF	chr17:38597098-38597918	SK-N-SH	brain:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
35	CTCF	chr17:38597244-38597553	Spleen_OC	spleen:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
36	CTCF	chr17:38595342-38595362	HepG2	liver:	n/a	n/a
37	CTCF	chr17:38595940-38596008	K562	blood:	n/a	n/a
38	CTCF	chr17:38597266-38597550	Pancreas_OC	pancreas:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
39	CTCF	chr17:38595320-38595470	GM12864	blood:	n/a	chr17:38595360-38595369
40	CTCF	chr17:38597217-38597618	ECC-1	luminal epithelium:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
41	CTCF	chr17:38597266-38597557	Hela-S3	cervix:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
42	CTCF	chr17:38597203-38597612	T-47D	breast:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
43	CTCF	chr17:38597173-38597619	H1-hESC	embryonic stem cell:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
44	CTCF	chr17:38595300-38595450	HUVEC	blood vessel:	n/a	chr17:38595360-38595369
45	CTCF	chr17:38595260-38595410	HBMEC	blood vessel:	n/a	chr17:38595360-38595369
46	CTCF	chr17:38595280-38595430	GM12866	blood:	n/a	chr17:38595360-38595369
47	CTCF	chr17:38597265-38597555	Gliobla	brain:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
48	CTCF	chr17:38597081-38597106	GM13976	blood:	n/a	n/a
49	CTCF	chr17:38597255-38597563	GM12891	blood:	n/a	chr17:38597403-38597421 chr17:38597443-38597451
50	CTCF	chr17:38596520-38596670	HEK293	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:38596324-38596374	Jurkat	blood:	n/a
2	chr17:38596324-38596374	NHDF-neo	bronchial:	n/a
3	chr17:38596324-38596374	U87	brain:	n/a
4	chr17:38596324-38596374	NHBE	bronchial:	n/a
5	chr17:38596324-38596374	ECC-1	luminal epithelium:	n/a
6	chr17:38596324-38596374	Hela-S3	cervix:	n/a
7	chr17:38596324-38596374	NT2-D1	testis:	n/a
8	chr17:38596324-38596374	SAEC	small airway:	n/a
9	chr17:38596324-38596374	AoSMC	blood vessel:	n/a
10	chr17:38596324-38596374	GM12891	blood:	n/a
11	chr17:38596324-38596374	HL-60	blood:	n/a
12	chr17:38596324-38596374	PFSK-1	brain:	n/a
13	chr17:38596324-38596374	HMEC	breast:	n/a
14	chr17:38596324-38596374	HIPEpiC	eye:	n/a
15	chr17:38596324-38596374	GM12892	blood:	n/a
16	chr17:38596324-38596374	AG09309	skin:	n/a
17	chr17:38596324-38596374	SK-N-SH	brain:	n/a
18	chr17:38596324-38596374	HUVEC	blood vessel:	n/a
19	chr17:38596324-38596374	AG04450	lung:	fetal
20	chr17:38596324-38596374	T-47D	breast:	n/a
21	chr17:38596324-38596374	HEK293	kidney:	embryo
22	chr17:38596324-38596374	IMR90	lung:	fetal
23	chr17:38596324-38596374	LNCaP	prostate:	n/a
24	chr17:38596324-38596374	CMK	blood:	n/a
25	chr17:38596324-38596374	PANC-1	pancreas:	n/a
26	chr17:38596324-38596374	SKMC	muscle:	n/a
27	chr17:38596324-38596374	ProgFib	skin:	n/a
28	chr17:38596324-38596374	MCF10A-Er-Src	breast:	n/a
29	chr17:38596324-38596374	K562	blood:	n/a
30	chr17:38596324-38596374	HRE	kidney:	n/a
31	chr17:38596324-38596374	RPTEC	kidney:	n/a
32	chr17:38596324-38596374	HAEpiC	amniotic membrane:	n/a
33	chr17:38596324-38596374	HCF	heart:	n/a
34	chr17:38596324-38596374	GM12878	blood:	n/a
35	chr17:38596324-38596374	Hepatocyte	liver:	n/a
36	chr17:38596324-38596374	GM19239	blood:	n/a
37	chr17:38596324-38596374	HRCEpiC	kidney:	n/a
38	chr17:38596324-38596374	AG04449	skin:	fetal
39	chr17:38596324-38596374	AG10803	skin:	n/a
40	chr17:38596324-38596374	BJ	skin:	n/a
41	chr17:38596324-38596374	NB4	blood:	n/a
42	chr17:38596324-38596374	GM06990	blood:	n/a
43	chr17:38596324-38596374	HCM	heart:	n/a
44	chr17:38596324-38596374	AG09319	gingival:	n/a
45	chr17:38596324-38596374	BE2_C	brain:	n/a
46	chr17:38596324-38596374	HEEpiC	esophagus:	n/a
47	chr17:38596324-38596374	A549	lung:	n/a
48	chr17:38596324-38596374	HCPEpiC	choroid plexus:	n/a
49	chr17:38596324-38596374	HepG2	liver:	n/a
50	chr17:38596324-38596374	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:38587923..38591705-chr17:38591977..38594441,3	MCF-7	breast:
2	chr17:38573492..38575865-chr17:38596037..38598385,2	K562	blood:
3	chr17:38596917..38597904-chr17:38689265..38690168,5	K562	blood:
4	chr17:38595131..38596069-chr17:38604686..38605482,2	MCF-7	breast:
5	chr17:38579876..38582624-chr17:38593992..38595822,2	K562	blood:
6	chr17:38456433..38460322-chr17:38596356..38599161,3	MCF-7	breast:
7	chr17:38593953..38595936-chr17:38603501..38605145,2	K562	blood:
8	chr17:38592886..38594691-chr17:38595993..38598092,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000240125	TF binding region
IGFBP4	TF binding region
ENSG00000240125	CpG island
IGFBP4	CpG island
ENSG00000270145	chromatin interactions
ENSG00000240125	chromatin interactions
ENSG00000131747	chromatin interactions

Extended variants
information (count: 117 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:117 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531546815	chr17:38594129-38594130	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs186238043	chr17:38594152-38594153	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs191158738	chr17:38594219-38594220	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs147606790	chr17:38594234-38594235	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs528033221	chr17:38594461-38594462	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs80168218	chr17:38594473-38594474	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs398030846	chr17:38594474-38594475	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs181376920	chr17:38594508-38594509	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs679266	chr17:38594513-38594514	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs566193358	chr17:38594536-38594537	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs142184336	chr17:38594570-38594571	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs555028411	chr17:38594598-38594599	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs146071033	chr17:38594601-38594602	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs543799773	chr17:38594606-38594607	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs559209269	chr17:38594607-38594608	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs577442646	chr17:38594614-38594615	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs207476403	chr17:38594615-38594616	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs186043153	chr17:38594647-38594648	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs190511560	chr17:38594651-38594652	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs112276968	chr17:38594676-38594677	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs527413820	chr17:38594709-38594710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537721404	chr17:38594750-38594751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542312167	chr17:38594754-38594755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11078945	chr17:38594756-38594757	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs201333694	chr17:38594777-38594778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183116128	chr17:38594780-38594781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs35103116	chr17:38594806-38594807	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs571539624	chr17:38594818-38594819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532271416	chr17:38594865-38594866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138931329	chr17:38594880-38594881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565857180	chr17:38594885-38594886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536787114	chr17:38594934-38594935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34307789	chr17:38594943-38594944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2469948	chr17:38595075-38595076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570120104	chr17:38595114-38595115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541168526	chr17:38595118-38595119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201917304	chr17:38595119-38595120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376267337	chr17:38595122-38595123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553431327	chr17:38595139-38595140	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs573104652	chr17:38595155-38595156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143438032	chr17:38595181-38595182	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs558648010	chr17:38595200-38595201	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs577502579	chr17:38595220-38595221	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs541342113	chr17:38595232-38595233	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs545237158	chr17:38595240-38595241	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs553198906	chr17:38595281-38595282	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs574682941	chr17:38595289-38595290	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs541979794	chr17:38595313-38595314	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs7212482	chr17:38595327-38595328	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs116984598	chr17:38595393-38595394	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
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
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
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	24379144	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
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Breast cancer	21509527	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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Urothelial carcinoma	21177765	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Disease	22962312	CNVD
Mental retardation	20152051	CNVD
Mental retardation	19951919	CNVD
Mental retardation	22817714	CNVD
Mental retardation	21956041	CNVD
Brain cancer	19584924	CNVD
Glioblastoma multiforme	22286061	CNVD
Schizophrenia	21399695	CNVD
Non-syndromic sensorineural hearing loss	19165922	CNVD
Prader-willi syndrome	20588305	CNVD
17q21.31 microdeletion syndrome	16940994	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
17q21.31 microdeletion syndrome	22283845	CNVD
Intellectual disability	22194194	CNVD
17q21.31 microdeletion syndrome	20606400	CNVD
17q21.31 microdeletion syndrome	18628315	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Malignant fibrous histiocytomas	21085701	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
Human papillomavirus	17975027	CNVD
Breast cancer	19767729	CNVD
Breast cancer	20409316	CNVD
Medulloblastoma	16783165	CNVD
Bladder cancer	21909424	CNVD
Intracranial arachnoid cysts	20187927	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:38579600-38598800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr17:38584600-38600200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr17:38589600-38598800	Weak transcription	Fetal Intestine Small	intestine
4	chr17:38589800-38598600	Weak transcription	NHDF-Ad	bronchial
5	chr17:38590200-38599000	Weak transcription	Lung	lung
6	chr17:38590400-38597400	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr17:38590400-38598600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr17:38590400-38598800	Weak transcription	Osteobl	bone
9	chr17:38590600-38596600	Weak transcription	A549	lung
10	chr17:38592600-38594200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr17:38592600-38594200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr17:38592600-38594200	Enhancers	Rectal Smooth Muscle	rectum
13	chr17:38592600-38594400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr17:38592600-38594600	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr17:38592800-38594200	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr17:38592800-38594200	Enhancers	Colon Smooth Muscle	Colon
17	chr17:38592800-38594200	Enhancers	Fetal Muscle Leg	muscle
18	chr17:38592800-38594400	Enhancers	K562	blood
19	chr17:38593000-38594200	Enhancers	Left Ventricle	heart
20	chr17:38593000-38594200	Enhancers	Right Ventricle	heart
21	chr17:38593000-38594400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr17:38593200-38594200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr17:38593200-38594200	Enhancers	Right Atrium	heart
24	chr17:38593200-38594200	Enhancers	Spleen	Spleen
25	chr17:38593200-38594200	Enhancers	HSMM	muscle
26	chr17:38593200-38594400	Enhancers	Adipose Nuclei	Adipose
27	chr17:38593200-38598800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr17:38593400-38594200	Enhancers	Primary hematopoietic stem cells	blood
29	chr17:38593400-38594200	Enhancers	Fetal Muscle Trunk	muscle
30	chr17:38593400-38594200	Enhancers	Fetal Stomach	stomach
31	chr17:38593400-38594200	Enhancers	Dnd41	blood
32	chr17:38593400-38594200	Bivalent Enhancer	NHEK	skin
33	chr17:38593400-38594400	Enhancers	GM12878-XiMat	blood
34	chr17:38593600-38594200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr17:38593600-38594200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr17:38593600-38594200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr17:38593600-38594200	Enhancers	Esophagus	oesophagus
38	chr17:38593600-38594200	Bivalent Enhancer	HepG2	liver
39	chr17:38593600-38598800	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr17:38593800-38594200	Enhancers	Fetal Thymus	thymus
41	chr17:38593800-38594400	Enhancers	Stomach Smooth Muscle	stomach
42	chr17:38593800-38597400	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr17:38593800-38598600	Weak transcription	HUVEC	blood vessel
44	chr17:38594000-38597200	Weak transcription	Primary B cells from peripheral blood	blood
45	chr17:38594000-38597400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr17:38594000-38597400	Weak transcription	Liver	Liver
47	chr17:38594000-38598600	Weak transcription	Placenta	Placenta
48	chr17:38594000-38598800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr17:38594000-38598800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr17:38594000-38598800	Weak transcription	Muscle Satellite Cultured Cells	--

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