Variant report

Variant	nsv524010
Chromosome Location	chr6:33468151-33505981
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:525)
CpG islands
(count:368)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:525 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:33479978-33480178	K562	blood:	n/a	n/a
2	ARID3A	chr6:33473487-33474127	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:33473977-33474136	K562	blood:	n/a	n/a
4	ATF1	chr6:33479897-33480276	K562	blood:	n/a	n/a
5	ATF1	chr6:33477590-33477686	K562	blood:	n/a	n/a
6	ATF2	chr6:33476039-33476493	GM12878	blood:	n/a	n/a
7	ATF2	chr6:33476098-33476485	GM12878	blood:	n/a	n/a
8	BATF	chr6:33476029-33476556	GM12878	blood:	n/a	n/a
9	BATF	chr6:33476075-33476456	GM12878	blood:	n/a	n/a
10	BCL11A	chr6:33476131-33476465	GM12878	blood:	n/a	n/a
11	BCL11A	chr6:33476040-33476490	GM12878	blood:	n/a	n/a
12	BCL3	chr6:33481131-33481620	GM12878	blood:	n/a	n/a
13	BCLAF1	chr6:33476085-33476487	GM12878	blood:	n/a	n/a
14	BCLAF1	chr6:33476575-33477150	GM12878	blood:	n/a	chr6:33476815-33476824
15	BCLAF1	chr6:33476075-33476507	GM12878	blood:	n/a	n/a
16	BHLHE40	chr6:33476123-33476636	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:33479940-33480218	K562	blood:	n/a	n/a
18	BHLHE40	chr6:33485081-33485211	K562	blood:	n/a	n/a
19	CBX3	chr6:33479810-33480243	K562	blood:	n/a	n/a
20	CCNT2	chr6:33479996-33480362	K562	blood:	n/a	chr6:33480073-33480093
21	CEBPB	chr6:33484491-33484869	MCF-7	breast:	n/a	chr6:33484686-33484697
22	CEBPB	chr6:33502527-33502711	K562	blood:	n/a	chr6:33502571-33502582
23	CEBPB	chr6:33479814-33479922	HepG2	liver:	n/a	chr6:33479876-33479887
24	CEBPB	chr6:33491624-33491936	HepG2	liver:	n/a	chr6:33491775-33491786
25	CEBPB	chr6:33479777-33480009	A549	lung:	n/a	chr6:33479876-33479887
26	CEBPB	chr6:33484536-33484779	A549	lung:	n/a	chr6:33484686-33484697
27	CEBPB	chr6:33484528-33484806	HepG2	liver:	n/a	chr6:33484686-33484697
28	CEBPB	chr6:33479756-33479951	K562	blood:	n/a	chr6:33479876-33479887
29	CEBPB	chr6:33502466-33502692	A549	lung:	n/a	chr6:33502571-33502582
30	CEBPB	chr6:33479794-33479994	H1-hESC	embryonic stem cell:	n/a	chr6:33479876-33479887
31	CEBPB	chr6:33479796-33480075	K562	blood:	n/a	chr6:33479876-33479887
32	CEBPB	chr6:33484602-33484802	K562	blood:	n/a	chr6:33484686-33484697
33	CEBPB	chr6:33484629-33484829	Hela-S3	cervix:	n/a	chr6:33484686-33484697
34	CEBPB	chr6:33491640-33491935	A549	lung:	n/a	chr6:33491775-33491786
35	CEBPB	chr6:33484596-33484770	HepG2	liver:	n/a	chr6:33484686-33484697
36	CEBPB	chr6:33502456-33502701	HepG2	liver:	n/a	chr6:33502571-33502582
37	CEBPB	chr6:33498944-33498955	K562	blood:	n/a	n/a
38	CEBPB	chr6:33499797-33500036	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr6:33484537-33484776	IMR90	lung:	n/a	chr6:33484686-33484697
40	CEBPB	chr6:33484529-33484853	K562	blood:	n/a	chr6:33484686-33484697
41	CEBPB	chr6:33479801-33479996	IMR90	lung:	n/a	chr6:33479876-33479887
42	CEBPB	chr6:33479800-33479999	Hela-S3	cervix:	n/a	chr6:33479876-33479887
43	CEBPB	chr6:33491645-33491910	K562	blood:	n/a	chr6:33491775-33491786
44	CEBPB	chr6:33499777-33500000	HepG2	liver:	n/a	n/a
45	CEBPB	chr6:33479773-33480086	K562	blood:	n/a	chr6:33479876-33479887
46	CEBPB	chr6:33484545-33484847	K562	blood:	n/a	chr6:33484686-33484697
47	CEBPB	chr6:33491647-33491915	IMR90	lung:	n/a	chr6:33491775-33491786
48	CHD2	chr6:33480058-33480248	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr6:33476223-33476457	GM12878	blood:	n/a	n/a
50	CREB1	chr6:33476133-33476391	GM12878	blood:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:33489501-33489551	U87	brain:	n/a
2	chr6:33489803-33489853	GM12878	blood:	n/a
3	chr6:33489501-33489551	U87	brain:	n/a
4	chr6:33489803-33489853	GM12878	blood:	n/a
5	chr6:33493156-33493206	A549	lung:	n/a
6	chr6:33489803-33489853	HRE	kidney:	n/a
7	chr6:33489501-33489551	H1-hESC	embryonic stem cell:	embryo
8	chr6:33489803-33489853	HEEpiC	esophagus:	n/a
9	chr6:33501379-33501429	GM06990	blood:	n/a
10	chr6:33470382-33470432	MCF-7	breast:	n/a
11	chr6:33470382-33470432	SAEC	small airway:	n/a
12	chr6:33489803-33489853	AoSMC	blood vessel:	n/a
13	chr6:33500486-33500536	AoSMC	blood vessel:	n/a
14	chr6:33500486-33500536	A549	lung:	n/a
15	chr6:33501379-33501429	U87	brain:	n/a
16	chr6:33500486-33500536	ECC-1	luminal epithelium:	n/a
17	chr6:33493156-33493206	HCT-116	colon:	n/a
18	chr6:33501379-33501429	HCPEpiC	choroid plexus:	n/a
19	chr6:33493156-33493206	HCF	heart:	n/a
20	chr6:33489501-33489551	IMR90	lung:	fetal
21	chr6:33493156-33493206	LNCaP	prostate:	n/a
22	chr6:33470382-33470432	ECC-1	luminal epithelium:	n/a
23	chr6:33470382-33470432	CMK	blood:	n/a
24	chr6:33470382-33470432	T-47D	breast:	n/a
25	chr6:33493156-33493206	HEK293	kidney:	embryo
26	chr6:33489803-33489853	A549	lung:	n/a
27	chr6:33501379-33501429	T-47D	breast:	n/a
28	chr6:33489501-33489551	RPTEC	kidney:	n/a
29	chr6:33470382-33470432	HCT-116	colon:	n/a
30	chr6:33489501-33489551	GM12878	blood:	n/a
31	chr6:33489501-33489551	NHBE	bronchial:	n/a
32	chr6:33489501-33489551	Caco-2	colon:	n/a
33	chr6:33470382-33470432	MCF10A-Er-Src	breast:	n/a
34	chr6:33493156-33493206	BE2_C	brain:	n/a
35	chr6:33500486-33500536	SK-N-SH_RA	brain:	n/a
36	chr6:33470382-33470432	BJ	skin:	n/a
37	chr6:33489501-33489551	NHDF-neo	bronchial:	n/a
38	chr6:33493156-33493206	NH-A	brain:	n/a
39	chr6:33500486-33500536	SKMC	muscle:	n/a
40	chr6:33470382-33470432	IMR90	lung:	fetal
41	chr6:33470382-33470432	HRPEpiC	eye:	n/a
42	chr6:33470382-33470432	SK-N-SH_RA	brain:	n/a
43	chr6:33470382-33470432	ProgFib	skin:	n/a
44	chr6:33489803-33489853	RPTEC	kidney:	n/a
45	chr6:33501379-33501429	AG09309	skin:	n/a
46	chr6:33489501-33489551	HNPCEpiC	eye:	n/a
47	chr6:33493156-33493206	HL-60	blood:	n/a
48	chr6:33489803-33489853	CMK	blood:	n/a
49	chr6:33500486-33500536	MCF10A-Er-Src	breast:	n/a
50	chr6:33470382-33470432	SK-N-MC	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:33463213..33467360-chr6:33468926..33472563,4	K562	blood:
2	chr6:33385003..33387538-chr6:33494085..33496852,2	K562	blood:
3	chr6:33483395..33487072-chr6:33487166..33490449,4	MCF-7	breast:
4	chr6:33480361..33482958-chr6:33629089..33631311,2	K562	blood:
5	chr6:33393869..33396201-chr6:33479107..33481448,2	MCF-7	breast:
6	chr6:33463213..33466886-chr6:33468926..33471484,3	K562	blood:
7	chr6:33479121..33484420-chr6:33487848..33490096,5	K562	blood:
8	chr6:33284016..33286661-chr6:33471005..33472744,2	K562	blood:
9	chr6:33479121..33484420-chr6:33487848..33490096,5	K562	blood:
10	chr6:33265668..33268001-chr6:33494684..33497652,2	MCF-7	breast:
11	chr6:33422288..33424743-chr6:33478570..33480571,2	MCF-7	breast:
12	chr6:33407586..33409275-chr6:33483578..33485423,2	K562	blood:
13	chr6:33445656..33447600-chr6:33486637..33489207,2	K562	blood:
14	chr6:33483395..33487072-chr6:33487166..33490449,4	MCF-7	breast:
15	chr6:33394909..33396953-chr6:33473800..33476253,2	MCF-7	breast:

No data

Variant related genes	Relation type
RN7SL26P	TF binding region
RN7SL26P	CpG island
ENSG00000237441	chromatin interactions
ENSG00000236104	chromatin interactions
ENSG00000112514	chromatin interactions
ENSG00000213588	chromatin interactions

Extended variants
information (count: 1608 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:1608 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11759461	chr6:33468151-33468152	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561381337	chr6:33468180-33468181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543710936	chr6:33468324-33468325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181711159	chr6:33468354-33468355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550887163	chr6:33468372-33468373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374264698	chr6:33468374-33468375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs4428487	chr6:33468394-33468395	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs533227928	chr6:33468451-33468452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551611519	chr6:33468524-33468525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144235672	chr6:33468621-33468622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9380363	chr6:33468633-33468634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533917996	chr6:33468649-33468650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186180631	chr6:33468653-33468654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191034131	chr6:33468654-33468655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543222160	chr6:33468674-33468675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs34633066	chr6:33468675-33468676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79191157	chr6:33468676-33468677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs397740390	chr6:33468687-33468688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201655035	chr6:33468688-33468689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534217555	chr6:33468735-33468736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371971386	chr6:33468757-33468758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs17682662	chr6:33468761-33468762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556097940	chr6:33468888-33468889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs578200248	chr6:33468927-33468928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs151114108	chr6:33468934-33468935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375528456	chr6:33468945-33468946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573658486	chr6:33469144-33469145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183346660	chr6:33469158-33469159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572302674	chr6:33469193-33469194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187766610	chr6:33469210-33469211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561212126	chr6:33469212-33469213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35322268	chr6:33469230-33469231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369851181	chr6:33469249-33469250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541148787	chr6:33469305-33469306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531760867	chr6:33469309-33469310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs35078385	chr6:33469432-33469433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190784449	chr6:33469443-33469444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565240811	chr6:33469491-33469492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372366191	chr6:33469551-33469552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141116375	chr6:33469565-33469566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs6942274	chr6:33469602-33469603	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs183088247	chr6:33469649-33469650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150239932	chr6:33469661-33469662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549088299	chr6:33469703-33469704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188134843	chr6:33469726-33469727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537913399	chr6:33469747-33469748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555898525	chr6:33469748-33469749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570865717	chr6:33469751-33469752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370974098	chr6:33469772-33469773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538994910	chr6:33469778-33469779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

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
Acute myeloid leukemia	20729466	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
Esophageal adenocarcinoma	18820669	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
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Myelofibrosis	22110671	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Encephalopathy	20692195	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Immune disease	17576883	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21781307	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD

Chromatin state (count:299 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33453000-33474000	Weak transcription	Right Atrium	heart
2	chr6:33468200-33469600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:33470000-33470800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:33470400-33470800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:33473200-33474000	Enhancers	HepG2	liver
6	chr6:33473400-33474200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:33473400-33474200	Enhancers	Adipose Nuclei	Adipose
8	chr6:33473400-33474400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:33473600-33473800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr6:33473600-33474200	Enhancers	Duodenum Mucosa	Duodenum
11	chr6:33473600-33474400	Enhancers	K562	blood
12	chr6:33473600-33474600	Enhancers	Fetal Heart	heart
13	chr6:33473800-33474400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr6:33473800-33476800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr6:33474000-33474200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr6:33474000-33474200	Bivalent Enhancer	HepG2	liver
17	chr6:33474000-33474400	Enhancers	Fetal Intestine Small	intestine
18	chr6:33474000-33474400	Enhancers	Right Atrium	heart
19	chr6:33474200-33474400	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr6:33474200-33476800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr6:33474200-33476800	Weak transcription	Adipose Nuclei	Adipose
22	chr6:33474200-33477000	Weak transcription	Duodenum Mucosa	Duodenum
23	chr6:33474400-33476800	Weak transcription	Right Atrium	heart
24	chr6:33474400-33476800	Weak transcription	K562	blood
25	chr6:33474400-33477000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr6:33474400-33481200	Weak transcription	Fetal Intestine Small	intestine
27	chr6:33474600-33477000	Weak transcription	Fetal Heart	heart
28	chr6:33475200-33476600	Enhancers	GM12878-XiMat	blood
29	chr6:33476000-33476200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
30	chr6:33476000-33477200	Enhancers	Primary B cells from peripheral blood	blood
31	chr6:33476200-33476400	Enhancers	Spleen	Spleen
32	chr6:33476200-33476600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr6:33476200-33476600	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr6:33476200-33476800	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr6:33476400-33476800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr6:33476400-33477000	Weak transcription	Spleen	Spleen
37	chr6:33476600-33476800	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr6:33476600-33476800	Enhancers	Primary B cells from cord blood	blood
39	chr6:33476600-33476800	Enhancers	Primary hematopoietic stem cells	blood
40	chr6:33476600-33476800	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr6:33476600-33476800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr6:33476600-33476800	Active TSS	Fetal Kidney	kidney
43	chr6:33476600-33477200	Flanking Active TSS	GM12878-XiMat	blood
44	chr6:33476600-33477600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr6:33476600-33477600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr6:33476600-33479800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr6:33476800-33477000	Enhancers	H1 Cell Line	embryonic stem cell
48	chr6:33476800-33477000	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr6:33476800-33477000	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr6:33476800-33477000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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