Variant report

Variant	nsv886765
Chromosome Location	chr6:150198491-150288722
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3137)
CpG islands
(count:5129)
Chromatin interactive
region (count:92)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:3137 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:150208597-150208770	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:150247364-150247671	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:150255239-150255664	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:150255309-150255597	K562	blood:	n/a	n/a
5	ARID3A	chr6:150284568-150285068	K562	blood:	n/a	n/a
6	ARID3A	chr6:150250882-150250933	K562	blood:	n/a	n/a
7	ARID3A	chr6:150216600-150216665	K562	blood:	n/a	n/a
8	ATF1	chr6:150262888-150263243	K562	blood:	n/a	n/a
9	ATF1	chr6:150255302-150256283	K562	blood:	n/a	n/a
10	ATF1	chr6:150284609-150285207	K562	blood:	n/a	n/a
11	ATF2	chr6:150259804-150260315	GM12878	blood:	n/a	n/a
12	ATF2	chr6:150259675-150260384	GM12878	blood:	n/a	n/a
13	ATF2	chr6:150255277-150255811	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr6:150255242-150255812	GM12878	blood:	n/a	n/a
15	ATF2	chr6:150255225-150255776	GM12878	blood:	n/a	n/a
16	ATF2	chr6:150284647-150285227	H1-hESC	embryonic stem cell:	n/a	chr6:150284985-150284996
17	ATF3	chr6:150284718-150285281	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr6:150284652-150285226	K562	blood:	n/a	n/a
19	ATF3	chr6:150284800-150285134	A549	lung:	n/a	n/a
20	ATF3	chr6:150284609-150285137	K562	blood:	n/a	n/a
21	ATF3	chr6:150284750-150285128	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF3	chr6:150284655-150285416	HCT-116	colon:	n/a	n/a
23	ATF3	chr6:150247403-150247668	K562	blood:	n/a	n/a
24	ATF3	chr6:150255382-150255760	K562	blood:	n/a	n/a
25	BACH1	chr6:150259845-150259973	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr6:150243580-150243643	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr6:150247368-150247568	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr6:150244559-150244801	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr6:150284433-150286779	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr6:150263349-150263435	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr6:150246818-150246841	H1-hESC	embryonic stem cell:	n/a	n/a
32	BATF	chr6:150259890-150260217	GM12878	blood:	n/a	n/a
33	BATF	chr6:150284202-150284490	GM12878	blood:	n/a	n/a
34	BATF	chr6:150275087-150275305	GM12878	blood:	n/a	n/a
35	BATF	chr6:150284861-150285131	GM12878	blood:	n/a	n/a
36	BATF	chr6:150282958-150283170	GM12878	blood:	n/a	n/a
37	BATF	chr6:150280757-150280957	GM12878	blood:	n/a	chr6:150280887-150280898 chr6:150280888-150280898
38	BATF	chr6:150247400-150247634	GM12878	blood:	n/a	n/a
39	BATF	chr6:150259147-150259360	GM12878	blood:	n/a	n/a
40	BCL11A	chr6:150259955-150260168	GM12878	blood:	n/a	n/a
41	BCL11A	chr6:150259860-150260315	GM12878	blood:	n/a	n/a
42	BCL3	chr6:150259901-150260245	GM12878	blood:	n/a	n/a
43	BCLAF1	chr6:150259802-150260312	GM12878	blood:	n/a	n/a
44	BHLHE40	chr6:150280710-150280916	GM12878	blood:	n/a	chr6:150280798-150280807
45	BHLHE40	chr6:150255397-150256072	K562	blood:	n/a	n/a
46	BHLHE40	chr6:150284844-150285177	GM12878	blood:	n/a	n/a
47	BHLHE40	chr6:150238023-150238354	K562	blood:	n/a	n/a
48	BHLHE40	chr6:150255862-150256159	GM12878	blood:	n/a	n/a
49	BHLHE40	chr6:150262692-150263290	K562	blood:	n/a	n/a
50	BHLHE40	chr6:150259646-150260401	GM12878	blood:	n/a	chr6:150259658-150259674

(count:5129 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150231942-150231992	HEK293	kidney:	embryo
2	chr6:150262771-150262821	ProgFib	skin:	n/a
3	chr6:150247246-150247296	NH-A	brain:	n/a
4	chr6:150217448-150217498	BE2_C	brain:	n/a
5	chr6:150238016-150238066	MCF-7	breast:	n/a
6	chr6:150231942-150231992	HEK293	kidney:	embryo
7	chr6:150262771-150262821	ProgFib	skin:	n/a
8	chr6:150247246-150247296	NH-A	brain:	n/a
9	chr6:150217448-150217498	BE2_C	brain:	n/a
10	chr6:150238016-150238066	MCF-7	breast:	n/a
11	chr6:150244597-150244647	HNPCEpiC	eye:	n/a
12	chr6:150231994-150232044	GM12892	blood:	n/a
13	chr6:150213234-150213284	Hepatocyte	liver:	n/a
14	chr6:150266173-150266223	ProgFib	skin:	n/a
15	chr6:150285475-150285525	H1-hESC	embryonic stem cell:	embryo
16	chr6:150263035-150263085	HRE	kidney:	n/a
17	chr6:150285139-150285189	LNCaP	prostate:	n/a
18	chr6:150262734-150262784	K562	blood:	n/a
19	chr6:150212725-150212775	PFSK-1	brain:	n/a
20	chr6:150209640-150209690	HNPCEpiC	eye:	n/a
21	chr6:150263488-150263538	HAEpiC	amniotic membrane:	n/a
22	chr6:150259930-150259980	RPTEC	kidney:	n/a
23	chr6:150274542-150274592	HRPEpiC	eye:	n/a
24	chr6:150263035-150263085	HCF	heart:	n/a
25	chr6:150232183-150232233	BE2_C	brain:	n/a
26	chr6:150255758-150255808	Hela-S3	cervix:	n/a
27	chr6:150285088-150285138	BJ	skin:	n/a
28	chr6:150255758-150255808	AG10803	skin:	n/a
29	chr6:150259930-150259980	AoSMC	blood vessel:	n/a
30	chr6:150282383-150282433	LNCaP	prostate:	n/a
31	chr6:150238164-150238214	GM12878	blood:	n/a
32	chr6:150247624-150247674	NH-A	brain:	n/a
33	chr6:150263354-150263404	GM12891	blood:	n/a
34	chr6:150286212-150286262	SK-N-SH	brain:	n/a
35	chr6:150259930-150259980	NH-A	brain:	n/a
36	chr6:150232183-150232233	HCT-116	colon:	n/a
37	chr6:150247246-150247296	SK-N-SH_RA	brain:	n/a
38	chr6:150275714-150275764	SK-N-SH	brain:	n/a
39	chr6:150285634-150285684	NHDF-neo	bronchial:	n/a
40	chr6:150263118-150263168	IMR90	lung:	fetal
41	chr6:150263354-150263404	BE2_C	brain:	n/a
42	chr6:150242469-150242519	GM12891	blood:	n/a
43	chr6:150244288-150244338	SKMC	muscle:	n/a
44	chr6:150245071-150245121	HepG2	liver:	n/a
45	chr6:150263354-150263404	Jurkat	blood:	n/a
46	chr6:150275880-150275930	HRCEpiC	kidney:	n/a
47	chr6:150211211-150211261	HMEC	breast:	n/a
48	chr6:150213172-150213222	SKMC	muscle:	n/a
49	chr6:150285168-150285218	RPTEC	kidney:	n/a
50	chr6:150232174-150232224	IMR90	lung:	fetal

(count:92 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:150215647..150217438-chr6:150221792..150223743,2	MCF-7	breast:
2	chr6:150198184..150200903-chr6:150202024..150204310,2	K562	blood:
3	chr6:150276089..150279846-chr6:150282631..150286651,4	MCF-7	breast:
4	chr6:150217021..150219534-chr6:150242538..150245487,2	MCF-7	breast:
5	chr6:150201367..150203467-chr6:150207974..150210289,2	MCF-7	breast:
6	chr6:150174743..150177102-chr6:150220611..150223139,2	MCF-7	breast:
7	chr6:150239646..150241708-chr6:150246246..150248253,2	K562	blood:
8	chr6:150250256..150251800-chr6:150252543..150254483,2	MCF-7	breast:
9	chr6:150154902..150156132-chr6:150246873..150248035,8	MCF-7	breast:
10	chr6:150212160..150213980-chr6:150214968..150218117,3	K562	blood:
11	chr6:150288130..150291946-chr6:150324543..150327440,3	MCF-7	breast:
12	chr6:150182735..150186007-chr6:150239527..150243180,4	MCF-7	breast:
13	chr6:150161696..150162308-chr6:150247065..150247811,2	MCF-7	breast:
14	chr6:150276072..150278660-chr6:150282863..150284944,2	K562	blood:
15	chr6:149846576..149848106-chr6:150258402..150260712,2	K562	blood:
16	chr6:150263150..150264777-chr6:150325600..150328449,2	MCF-7	breast:
17	chr6:150237859..150240008-chr6:150242454..150244236,2	K562	blood:
18	chr6:150204116..150206853-chr6:150221041..150222804,2	K562	blood:
19	chr6:150183832..150186232-chr6:150215270..150224001,9	MCF-7	breast:
20	chr6:150195717..150198563-chr6:150225615..150228061,2	K562	blood:
21	chr6:150254783..150257862-chr6:150259479..150262603,4	K562	blood:
22	chr6:150181490..150187274-chr6:150243970..150248410,8	MCF-7	breast:
23	chr6:150226570..150229723-chr6:150237444..150240125,3	K562	blood:
24	chr6:150250322..150251340-chr6:150337738..150338572,3	K562	blood:
25	chr6:150182126..150186554-chr6:150208101..150210542,3	K562	blood:
26	chr6:150155297..150157506-chr6:150246299..150249094,2	K562	blood:
27	chr6:150153805..150156797-chr6:150246692..150249094,2	K562	blood:
28	chr6:150286967..150289038-chr6:150325599..150328579,2	K562	blood:
29	chr6:150250256..150251800-chr6:150252543..150254483,2	MCF-7	breast:
30	chr6:150286573..150288463-chr6:150317408..150319689,2	K562	blood:
31	chr6:150225385..150227618-chr6:150231399..150233931,2	MCF-7	breast:
32	chr6:150235746..150238768-chr6:150240556..150244338,4	MCF-7	breast:
33	chr6:150255165..150257260-chr6:150258635..150261924,3	MCF-7	breast:
34	chr6:150195717..150198563-chr6:150225615..150228061,2	K562	blood:
35	chr6:150239646..150241708-chr6:150246246..150248253,2	K562	blood:
36	chr6:150243800..150245856-chr6:150245979..150247636,2	MCF-7	breast:
37	chr6:150208190..150211087-chr6:150219720..150221224,2	MCF-7	breast:
38	chr6:150258514..150260378-chr6:150337573..150339969,2	MCF-7	breast:
39	chr6:150155391..150156182-chr6:150239663..150240372,2	MCF-7	breast:
40	chr6:150284327..150286937-chr6:150287191..150290217,6	K562	blood:
41	chr6:150225385..150227618-chr6:150231399..150233931,2	MCF-7	breast:
42	chr6:150183487..150185383-chr6:150249575..150251889,2	MCF-7	breast:
43	chr6:150185187..150186828-chr6:150215109..150217579,2	MCF-7	breast:
44	chr6:150238077..150241849-chr6:150242731..150245993,5	MCF-7	breast:
45	chr6:150274811..150275321-chr6:150336040..150336549,2	MCF-7	breast:
46	chr12:120730015..120730787-chr6:150215970..150216651,2	Hela-S3	cervix:
47	chr6:150281848..150284809-chr6:150294278..150296186,2	MCF-7	breast:
48	chr6:150155818..150157641-chr6:150245238..150247988,3	MCF-7	breast:
49	chr6:150287137..150289834-chr6:150291906..150294473,3	K562	blood:
50	chr6:150205939..150207450-chr6:150209753..150212132,2	K562	blood:

(count:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ULBP2-2	chr6:150256604-150256715	XLOC_005500
2	lnc-ULBP2-3	chr6:150217269-150217376	ENSG00000223701.1
3	lnc-ULBP2-3	chr6:150240323-150240644	ENSG00000223701.3
4	lnc-ULBP2-1	chr6:150261044-150262631	XLOC_005501
5	lnc-ULBP2-3	chr6:150240323-150240642	ENSG00000223701.3
6	lnc-RAET1E-1	chr6:150221505-150221774	expReg_chr6_11269_-
7	lnc-ULBP2-2	chr6:150255722-150255915	XLOC_005500
8	lnc-ULBP2-2	chr6:150255650-150255915	NONHSAT115522
9	lnc-ULBP2-1	chr6:150260558-150260871	XLOC_005501
10	lnc-ULBP2-2	chr6:150256604-150257152	ENSG00000216621.3
11	lnc-ULBP2-3	chr6:150240323-150240583	NONHSAT115517
12	lnc-ULBP2-2	chr6:150255663-150255915	ENSG00000216621.3
13	lnc-ULBP2-1	chr6:150260453-150260658	XLOC_005501
14	lnc-RAET1G-1	chr6:150219157-150219213	NONHSAT115520
15	lnc-RAET1G-1	chr6:150216615-150217168	NONHSAT115520
16	lnc-ULBP2-3	chr6:150211239-150211300	ENSG00000223701.1
17	lnc-ULBP2-3	chr6:150217269-150217375	NONHSAT115517
18	lnc-ULBP2-2	chr6:150256604-150257449	NONHSAT115522
19	lnc-ULBP2-3	chr6:150240323-150240644	ENSG00000223701.1
20	lnc-ULBP2-3	chr6:150205461-150205556	NONHSAT115516
21	lnc-ULBP2-3	chr6:150206721-150206809	ENSG00000223701.3
22	lnc-ULBP2-4	chr6:150272969-150273375	NONHSAT115528
23	lnc-ULBP2-3	chr6:150205468-150205591	NONHSAT115517
24	lnc-ULBP2-3	chr6:150217269-150217375	ENSG00000223701.3
25	lnc-ULBP2-3	chr6:150205567-150205591	ENSG00000223701.3
26	lnc-ULBP2-2	chr6:150257843-150257918	NONHSAT115524
27	lnc-ULBP2-1	chr6:150261044-150262631	XLOC_005501
28	lnc-ULBP2-2	chr6:150257101-150257464	NONHSAT115524
29	lnc-ULBP2-1	chr6:150260117-150260140	NONHSAT115525
30	lnc-ULBP2-3	chr6:150211239-150211300	ENSG00000223701.3
31	lnc-ULBP2-3	chr6:150206721-150206809	NONHSAT115517
32	lnc-ULBP2-1	chr6:150261044-150262766	NONHSAT115525

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ULBP2	hsa-miR-34c-5p	chr6:150269988-150270008
2	ULBP2	hsa-miR-34a-5p	chr6:150269987-150270008

Variant related genes	Relation type
CCT7P1	TF binding region
RAET1E	TF binding region
ENSG00000215094	TF binding region
RAET1E-AS1	TF binding region
ULBP2	TF binding region
RAET1G	TF binding region
ENSG00000216906	TF binding region
ULBP1	TF binding region
ENSG00000216621	TF binding region
CCT7P1	CpG island
RAET1E	CpG island
ENSG00000215094	CpG island
RAET1E-AS1	CpG island
ULBP2	CpG island
RAET1G	CpG island
ENSG00000216906	CpG island
ULBP1	CpG island
ENSG00000216621	CpG island
ENSG00000055211	chromatin interactions
ENSG00000217733	chromatin interactions
ENSG00000218358	chromatin interactions
ENSG00000111981	chromatin interactions
ENSG00000223701	chromatin interactions
ENSG00000203722	chromatin interactions
ENSG00000131015	chromatin interactions
ENSG00000164520	chromatin interactions
ENSG00000216621	chromatin interactions
ENSG00000268592	chromatin interactions
ENSG00000218510	chromatin interactions
ENSG00000120256	chromatin interactions
ENSG00000131013	chromatin interactions
SKI	miRNA target sites
ARID1B	miRNA target sites
ZNF236	miRNA target sites
VPS36	miRNA target sites
ZNF238	miRNA target sites
ARID1A	miRNA target sites

Extended variants
information (count: 4412 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:4412 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9322227	chr6:150198491-150198492	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs528893253	chr6:150198510-150198511	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs6910351	chr6:150198615-150198616	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs556429492	chr6:150198636-150198637	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs576473073	chr6:150198662-150198663	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs962218	chr6:150198673-150198674	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs558729969	chr6:150198676-150198677	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs572280104	chr6:150198761-150198762	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs145527717	chr6:150198776-150198777	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs148848147	chr6:150198782-150198783	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs58607113	chr6:150198788-150198789	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs145307417	chr6:150198845-150198846	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs558645037	chr6:150198846-150198847	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs543394355	chr6:150198854-150198855	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs531866444	chr6:150198866-150198867	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs532235362	chr6:150198871-150198872	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs137885513	chr6:150198900-150198901	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs117801422	chr6:150198922-150198923	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs184835610	chr6:150198948-150198949	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs548530350	chr6:150198965-150198966	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs568341429	chr6:150198985-150198986	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs190127589	chr6:150199015-150199016	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs571501984	chr6:150199105-150199106	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs578099352	chr6:150199191-150199192	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs538772620	chr6:150199204-150199205	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs558595790	chr6:150199205-150199206	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs140772135	chr6:150199234-150199235	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs369708999	chr6:150199354-150199355	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs60475279	chr6:150199357-150199358	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs9397049	chr6:150199430-150199431	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs543708820	chr6:150199473-150199474	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs145904877	chr6:150199474-150199475	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs76720740	chr6:150199517-150199518	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs527589613	chr6:150199523-150199524	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs545954561	chr6:150199541-150199542	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs559467017	chr6:150199542-150199543	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs181838929	chr6:150199543-150199544	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs374858624	chr6:150199544-150199545	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs561690858	chr6:150199545-150199546	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs536671654	chr6:150199554-150199555	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs115402242	chr6:150199595-150199596	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs386706960	chr6:150199616-150199617	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs141962911	chr6:150199617-150199618	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs371429474	chr6:150199630-150199631	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs549872661	chr6:150199651-150199652	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs59485028	chr6:150199684-150199685	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs373002924	chr6:150199695-150199696	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs532357907	chr6:150199752-150199753	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs141130613	chr6:150199833-150199834	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs201622938	chr6:150199840-150199841	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2541 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150197600-150198800	Enhancers	NHDF-Ad	bronchial
2	chr6:150198000-150205200	Weak transcription	Esophagus	oesophagus
3	chr6:150201400-150202600	Enhancers	Ovary	ovary
4	chr6:150202000-150202600	Enhancers	Right Atrium	heart
5	chr6:150202200-150202600	Enhancers	Pancreas	Pancrea
6	chr6:150202400-150202600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr6:150202400-150202800	Enhancers	HSMMtube	muscle
8	chr6:150202600-150205200	Weak transcription	Right Atrium	heart
9	chr6:150202600-150205400	Weak transcription	Ovary	ovary
10	chr6:150202800-150208600	Weak transcription	HSMMtube	muscle
11	chr6:150204200-150206800	Weak transcription	Hela-S3	cervix
12	chr6:150205000-150205200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr6:150205000-150205200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr6:150205000-150205200	Enhancers	A549	lung
15	chr6:150205000-150205200	Bivalent Enhancer	HepG2	liver
16	chr6:150205000-150205200	Enhancers	NHEK	skin
17	chr6:150205000-150205400	Enhancers	Duodenum Mucosa	Duodenum
18	chr6:150205000-150205800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr6:150205000-150205800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr6:150205000-150205800	Enhancers	Fetal Lung	lung
21	chr6:150205000-150206000	Enhancers	NHLF	lung
22	chr6:150205000-150210400	Enhancers	HMEC	breast
23	chr6:150205200-150205400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
24	chr6:150205200-150205400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
25	chr6:150205200-150205400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr6:150205200-150205400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
27	chr6:150205200-150205400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr6:150205200-150205400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr6:150205200-150205400	Enhancers	Esophagus	oesophagus
30	chr6:150205200-150205400	Active TSS	Right Atrium	heart
31	chr6:150205200-150205400	Flanking Active TSS	NHEK	skin
32	chr6:150205200-150205600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
33	chr6:150205200-150205600	Enhancers	Placenta	Placenta
34	chr6:150205200-150205600	Enhancers	NHDF-Ad	bronchial
35	chr6:150205200-150205800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr6:150205200-150205800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr6:150205200-150205800	Enhancers	Stomach Smooth Muscle	stomach
38	chr6:150205200-150205800	Bivalent Enhancer	K562	blood
39	chr6:150205200-150206000	Enhancers	Adipose Nuclei	Adipose
40	chr6:150205400-150205600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr6:150205400-150205600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr6:150205400-150205600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr6:150205400-150205600	Enhancers	Fetal Intestine Small	intestine
44	chr6:150205400-150205600	Bivalent Enhancer	Fetal Stomach	stomach
45	chr6:150205400-150205600	Flanking Active TSS	Right Atrium	heart
46	chr6:150205400-150205600	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr6:150205400-150205600	Enhancers	NHEK	skin
48	chr6:150205400-150205800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
49	chr6:150205400-150205800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
50	chr6:150205400-150205800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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