Variant report

Variant	nsv527115
Chromosome Location	chr6:28185726-28186554
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:300)
CpG islands
(count:183)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:300 , 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	BHLHE40	chr6:28186381-28186498	K562	blood:	n/a	n/a
2	CBX3	chr6:28186019-28187055	K562	blood:	n/a	n/a
3	CCNT2	chr6:28186380-28186975	K562	blood:	n/a	chr6:28186758-28186767 chr6:28186618-28186627
4	CEBPD	chr6:28186344-28186960	HepG2	liver:	n/a	n/a
5	CEBPD	chr6:28186534-28187061	K562	blood:	n/a	n/a
6	CHD1	chr6:28186456-28186619	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr6:28186433-28186982	Hela-S3	cervix:	n/a	chr6:28186764-28186774 chr6:28186722-28186732
8	CHD2	chr6:28185999-28186967	GM12878	blood:	n/a	chr6:28186764-28186774 chr6:28186722-28186732
9	CHD2	chr6:28186519-28186641	HepG2	liver:	n/a	n/a
10	CTCF	chr6:28186480-28186630	GM12867	blood:	n/a	chr6:28186586-28186599
11	CTCF	chr6:28186400-28186550	GM12875	blood:	n/a	n/a
12	CTCF	chr6:28186417-28186536	GM19239	blood:	n/a	n/a
13	CTCF	chr6:28186421-28186562	GM12892	blood:	n/a	n/a
14	CTCF	chr6:28186421-28186528	MCF-7	breast:	n/a	n/a
15	CTCF	chr6:28186395-28186566	MCF-7	breast:	n/a	n/a
16	CTCF	chr6:28186425-28186527	MCF-7	breast:	n/a	n/a
17	CTCF	chr6:28186380-28186530	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr6:28186434-28186521	GM10266	blood:	n/a	n/a
19	CTCF	chr6:28186420-28186570	HepG2	liver:	n/a	n/a
20	CTCF	chr6:28186500-28186650	NHEK	skin:	n/a	chr6:28186586-28186599
21	CTCF	chr6:28186319-28186641	K562	blood:	n/a	chr6:28186586-28186599
22	CTCF	chr6:28186442-28186559	GM12878	blood:	n/a	n/a
23	CTCF	chr6:28186279-28186676	K562	blood:	n/a	chr6:28186586-28186599
24	CTCF	chr6:28186400-28186550	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr6:28186423-28186572	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr6:28186280-28186430	NB4	blood:	n/a	n/a
27	CTCF	chr6:28186360-28186510	Caco-2	colon:	n/a	n/a
28	CTCF	chr6:28186460-28186610	Caco-2	colon:	n/a	chr6:28186586-28186599
29	CTCF	chr6:28186480-28186630	HCPEpiC	choroid plexus:	n/a	chr6:28186586-28186599
30	CTCF	chr6:28186420-28186570	GM06990	blood:	n/a	n/a
31	CTCF	chr6:28186380-28186530	GM12865	blood:	n/a	n/a
32	CTCF	chr6:28186440-28186590	HRE	kidney:	n/a	n/a
33	CTCF	chr6:28186380-28186530	AG04449	skin:	n/a	n/a
34	CTCF	chr6:28186360-28186510	GM12869	blood:	n/a	n/a
35	CTCF	chr6:28186480-28186630	GM12865	blood:	n/a	chr6:28186586-28186599
36	CTCF	chr6:28186380-28186530	GM12871	blood:	n/a	n/a
37	CTCF	chr6:28186306-28186881	GM12878	blood:	n/a	chr6:28186586-28186599
38	CTCF	chr6:28186426-28186536	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:28186336-28186662	K562	blood:	n/a	chr6:28186586-28186599
40	CTCF	chr6:28186440-28186590	GM12874	blood:	n/a	n/a
41	CTCF	chr6:28186406-28186574	MCF-7	breast:	n/a	n/a
42	CTCF	chr6:28186400-28186550	HCFaa	heart:	n/a	n/a
43	CTCF	chr6:28186460-28186610	GM12878	blood:	n/a	chr6:28186586-28186599
44	CTCF	chr6:28186406-28186564	GM19238	blood:	n/a	n/a
45	CTCF	chr6:28186280-28186430	BJ	skin:	n/a	n/a
46	CTCF	chr6:28186400-28186550	HEK293	kidney:	n/a	n/a
47	CTCF	chr6:28186404-28186567	GM12891	blood:	n/a	n/a
48	CTCF	chr6:28186401-28186562	GM19240	blood:	n/a	n/a
49	CTCF	chr6:28186445-28186495	A549	lung:	n/a	n/a
50	E2F6	chr6:28186339-28187250	A549	lung:	n/a	chr6:28186865-28186877 chr6:28186765-28186774 chr6:28186758-28186767

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:28185726-28185776	U87	brain:	n/a
2	chr6:28186447-28186497	IMR90	lung:	fetal
3	chr6:28186477-28186527	RPTEC	kidney:	n/a
4	chr6:28186447-28186497	HMEC	breast:	n/a
5	chr6:28185726-28185776	AoSMC	blood vessel:	n/a
6	chr6:28186447-28186497	HPAEpiC	pulmonary alveolar:	n/a
7	chr6:28186447-28186497	HIPEpiC	eye:	n/a
8	chr6:28186447-28186497	RPTEC	kidney:	n/a
9	chr6:28185726-28185776	Hela-S3	cervix:	n/a
10	chr6:28186447-28186497	MCF-7	breast:	n/a
11	chr6:28185726-28185776	GM12891	blood:	n/a
12	chr6:28186447-28186497	Hepatocyte	liver:	n/a
13	chr6:28186477-28186527	HepG2	liver:	n/a
14	chr6:28185726-28185776	SAEC	small airway:	n/a
15	chr6:28186477-28186527	ovcar-3	ovarian:	n/a
16	chr6:28185726-28185776	BJ	skin:	n/a
17	chr6:28185726-28185776	SKMC	muscle:	n/a
18	chr6:28186477-28186527	PANC-1	pancreas:	n/a
19	chr6:28186447-28186497	GM12878	blood:	n/a
20	chr6:28186447-28186497	T-47D	breast:	n/a
21	chr6:28185726-28185776	HCF	heart:	n/a
22	chr6:28186477-28186527	HEK293	kidney:	embryo
23	chr6:28186477-28186527	NHBE	bronchial:	n/a
24	chr6:28186447-28186497	HCT-116	colon:	n/a
25	chr6:28186477-28186527	MCF10A-Er-Src	breast:	n/a
26	chr6:28186477-28186527	SK-N-MC	brain:	n/a
27	chr6:28185726-28185776	Jurkat	blood:	n/a
28	chr6:28186477-28186527	HRE	kidney:	n/a
29	chr6:28186477-28186527	ProgFib	skin:	n/a
30	chr6:28186447-28186497	GM19239	blood:	n/a
31	chr6:28186447-28186497	ovcar-3	ovarian:	n/a
32	chr6:28185726-28185776	H1-hESC	embryonic stem cell:	embryo
33	chr6:28186477-28186527	AoSMC	blood vessel:	n/a
34	chr6:28186477-28186527	SK-N-SH_RA	brain:	n/a
35	chr6:28186477-28186527	HNPCEpiC	eye:	n/a
36	chr6:28186477-28186527	SK-N-SH	brain:	n/a
37	chr6:28186477-28186527	HUVEC	blood vessel:	n/a
38	chr6:28186447-28186497	NH-A	brain:	n/a
39	chr6:28186447-28186497	NB4	blood:	n/a
40	chr6:28185726-28185776	HNPCEpiC	eye:	n/a
41	chr6:28186447-28186497	NHDF-neo	bronchial:	n/a
42	chr6:28185726-28185776	AG04450	lung:	fetal
43	chr6:28185726-28185776	GM12878	blood:	n/a
44	chr6:28185726-28185776	HRPEpiC	eye:	n/a
45	chr6:28185726-28185776	A549	lung:	n/a
46	chr6:28186447-28186497	AG10803	skin:	n/a
47	chr6:28186447-28186497	Hela-S3	cervix:	n/a
48	chr6:28186447-28186497	HCM	heart:	n/a
49	chr6:28186477-28186527	GM06990	blood:	n/a
50	chr6:28186447-28186497	GM12891	blood:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:28184931..28189194-chr6:28190077..28194573,12	MCF-7	breast:
2	chr6:28182735..28195387-chr6:28315960..28325841,32	K562	blood:
3	chr6:28183629..28195178-chr6:28316250..28325659,29	K562	blood:
4	chr6:28184981..28190782-chr6:28297491..28307222,23	K562	blood:
5	chr6:28185564..28187470-chr6:28218621..28220714,2	MCF-7	breast:
6	chr6:28184339..28187958-chr6:28190844..28194750,7	MCF-7	breast:
7	chr6:28184440..28186086-chr6:28227732..28230449,2	K562	blood:
8	chr6:28182366..28191375-chr6:28300021..28306741,17	K562	blood:
9	chr6:28184805..28186411-chr6:28255755..28258597,2	K562	blood:
10	chr6:27805809..27807448-chr6:28184413..28187037,2	MCF-7	breast:
11	chr6:27774472..27777190-chr6:28183511..28185747,2	K562	blood:
12	chr6:28103775..28113920-chr6:28177995..28190115,32	K562	blood:
13	chr6:28186460..28191177-chr6:28246836..28252039,7	K562	blood:
14	chr6:28102723..28113786-chr6:28183725..28194756,41	K562	blood:
15	chr6:28143030..28145517-chr6:28186267..28188999,2	K562	blood:
16	chr6:28184789..28191313-chr6:28230652..28235913,7	K562	blood:
17	chr6:28100317..28107200-chr6:28184436..28191088,8	MCF-7	breast:
18	chr6:28104139..28106070-chr6:28185714..28187223,2	MCF-7	breast:
19	chr6:27775362..27779371-chr6:28186093..28189957,4	K562	blood:
20	chr6:28108272..28111912-chr6:28184259..28187979,3	MCF-7	breast:

No data

Variant related genes	Relation type
TOB2P1	TF binding region
TOB2P1	CpG island
ENSG00000217862	chromatin interactions
ENSG00000198315	chromatin interactions
ENSG00000189298	chromatin interactions
ENSG00000269293	chromatin interactions
ENSG00000196747	chromatin interactions
ENSG00000184348	chromatin interactions
ENSG00000261839	chromatin interactions
ENSG00000203813	chromatin interactions
ENSG00000137185	chromatin interactions
ENSG00000216901	chromatin interactions
ENSG00000233822	chromatin interactions
ENSG00000235109	chromatin interactions
ENSG00000187626	chromatin interactions
ENSG00000137338	chromatin interactions
ENSG00000185130	chromatin interactions
ENSG00000197062	chromatin interactions

Extended variants
information (count: 25 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1233664	chr6:28185726-28185727	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs527514687	chr6:28185801-28185802	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
3	rs143525255	chr6:28185822-28185823	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
4	rs72849213	chr6:28185922-28185923	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
5	rs563922209	chr6:28185962-28185963	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs533095724	chr6:28185970-28185971	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs549659255	chr6:28185994-28185995	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs569158868	chr6:28186008-28186009	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs538196282	chr6:28186029-28186030	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
10	rs572378946	chr6:28186030-28186031	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs374351573	chr6:28186053-28186054	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs534272597	chr6:28186077-28186078	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
13	rs554448759	chr6:28186080-28186081	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs577512124	chr6:28186092-28186093	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs367851927	chr6:28186125-28186126	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
16	rs367886749	chr6:28186204-28186205	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
17	rs556776697	chr6:28186243-28186244	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
18	rs148940952	chr6:28186322-28186323	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
19	rs541780255	chr6:28186354-28186355	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
20	rs193094893	chr6:28186355-28186356	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
21	rs572139447	chr6:28186357-28186358	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
22	rs540714952	chr6:28186412-28186413	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
23	rs563984141	chr6:28186416-28186417	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
24	rs371289317	chr6:28186448-28186449	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
25	rs1736894	chr6:28186554-28186555	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	16 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:102)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
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
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
Bipolar disorder	19114987	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:256 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:28180800-28186400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:28181400-28186000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:28181400-28186000	Weak transcription	HSMM	muscle
4	chr6:28182800-28186000	Enhancers	Placenta	Placenta
5	chr6:28183600-28186000	Weak transcription	HMEC	breast
6	chr6:28183600-28186200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr6:28183800-28185800	Enhancers	HepG2	liver
8	chr6:28184000-28185800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr6:28184000-28186000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:28184000-28186000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr6:28184200-28185800	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr6:28184600-28186000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
13	chr6:28184600-28186600	Enhancers	Spleen	Spleen
14	chr6:28184800-28185800	Enhancers	Right Ventricle	heart
15	chr6:28184800-28186000	Bivalent Enhancer	Fetal Muscle Leg	muscle
16	chr6:28184800-28186200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:28184800-28186400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
18	chr6:28185000-28186000	Weak transcription	Gastric	stomach
19	chr6:28185000-28186000	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr6:28185200-28185800	Bivalent Enhancer	Primary hematopoietic stem cells	blood
21	chr6:28185200-28186000	Enhancers	Fetal Heart	heart
22	chr6:28185200-28186000	Weak transcription	Right Atrium	heart
23	chr6:28185200-28186400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
24	chr6:28185400-28185800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr6:28185400-28185800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr6:28185400-28186000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr6:28185400-28186000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
28	chr6:28185400-28186000	Enhancers	Left Ventricle	heart
29	chr6:28185400-28186200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr6:28185400-28186200	Flanking Active TSS	K562	blood
31	chr6:28185400-28186400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr6:28185400-28186400	ZNF genes & repeats	Fetal Intestine Small	intestine
33	chr6:28185600-28185800	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr6:28185600-28185800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr6:28185600-28185800	Enhancers	Esophagus	oesophagus
36	chr6:28185600-28186000	Enhancers	GM12878-XiMat	blood
37	chr6:28185600-28186200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr6:28185600-28186400	Flanking Active TSS	Hela-S3	cervix
39	chr6:28185600-28186600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr6:28185600-28187000	Active TSS	H9 Cell Line	embryonic stem cell
41	chr6:28185600-28187400	Active TSS	Stomach Smooth Muscle	stomach
42	chr6:28185800-28186000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr6:28185800-28186000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
44	chr6:28185800-28186000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
45	chr6:28185800-28186000	Bivalent/Poised TSS	Primary T killer memory cells from peripheral blood	blood
46	chr6:28185800-28186000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr6:28185800-28186000	Enhancers	Adipose Nuclei	Adipose
48	chr6:28185800-28186000	Bivalent Enhancer	Brain Anterior Caudate	brain
49	chr6:28185800-28186000	Bivalent Enhancer	Brain Cingulate Gyrus	brain
50	chr6:28185800-28186000	Active TSS	Fetal Lung	lung

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