Variant report

Variant	nsv1058796
Chromosome Location	chr18:254290-313208
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	ARID3A	chr18:267953-268346	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:286488-286736	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:268051-268209	K562	blood:	n/a	n/a
4	ARID3A	chr18:269422-269886	HepG2	liver:	n/a	n/a
5	ATF1	chr18:267856-268252	K562	blood:	n/a	n/a
6	ATF2	chr18:267806-268299	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr18:267857-268299	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr18:267573-268458	GM12878	blood:	n/a	n/a
9	ATF2	chr18:267677-268450	GM12878	blood:	n/a	n/a
10	ATF3	chr18:267819-268244	K562	blood:	n/a	chr18:268062-268075 chr18:268064-268072 chr18:268065-268072 chr18:268061-268076 chr18:268062-268075 chr18:268062-268072 chr18:268061-268074 chr18:268062-268072 chr18:268053-268073 chr18:268061-268072 chr18:268062-268073
11	ATF3	chr18:267904-268183	GM12878	blood:	n/a	chr18:268062-268075 chr18:268064-268072 chr18:268065-268072 chr18:268061-268076 chr18:268062-268075 chr18:268062-268072 chr18:268061-268074 chr18:268062-268072 chr18:268053-268073 chr18:268061-268072 chr18:268062-268073
12	ATF3	chr18:267854-268179	HepG2	liver:	n/a	chr18:268062-268075 chr18:268064-268072 chr18:268065-268072 chr18:268061-268076 chr18:268062-268075 chr18:268062-268072 chr18:268061-268074 chr18:268062-268072 chr18:268053-268073 chr18:268061-268072 chr18:268062-268073
13	ATF3	chr18:267842-268358	GM12878	blood:	n/a	chr18:268062-268075 chr18:268064-268072 chr18:268065-268072 chr18:268061-268076 chr18:268062-268075 chr18:268062-268072 chr18:268061-268074 chr18:268062-268072 chr18:268053-268073 chr18:268061-268072 chr18:268062-268073
14	ATF3	chr18:267636-268296	H1-hESC	embryonic stem cell:	n/a	chr18:268062-268075 chr18:268064-268072 chr18:268065-268072 chr18:268061-268076 chr18:268062-268075 chr18:268062-268072 chr18:268061-268074 chr18:268062-268072 chr18:268053-268073 chr18:268061-268072 chr18:268062-268073
15	ATF3	chr18:267910-268154	H1-hESC	embryonic stem cell:	n/a	chr18:268062-268075 chr18:268064-268072 chr18:268065-268072 chr18:268061-268076 chr18:268062-268075 chr18:268062-268072 chr18:268061-268074 chr18:268062-268072 chr18:268053-268073 chr18:268061-268072 chr18:268062-268073
16	BACH1	chr18:267979-268355	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr18:267919-268509	GM12878	blood:	n/a	n/a
18	BCL11A	chr18:267902-268405	GM12878	blood:	n/a	chr18:268153-268162 chr18:268049-268062
19	BCL3	chr18:267887-268393	GM12878	blood:	n/a	chr18:268153-268162 chr18:268049-268062
20	BCL3	chr18:267839-268276	A549	lung:	n/a	chr18:268153-268162 chr18:268049-268062
21	BCL3	chr18:267793-268331	A549	lung:	n/a	chr18:268153-268162 chr18:268049-268062
22	BCLAF1	chr18:267804-269077	GM12878	blood:	n/a	chr18:268153-268162 chr18:268049-268062
23	BCLAF1	chr18:267773-268502	GM12878	blood:	n/a	chr18:268153-268162 chr18:268049-268062
24	BHLHE40	chr18:267852-268323	HepG2	liver:	n/a	chr18:268046-268062 chr18:268047-268063
25	BHLHE40	chr18:268183-268376	A549	lung:	n/a	n/a
26	BHLHE40	chr18:267862-268321	K562	blood:	n/a	chr18:268046-268062 chr18:268047-268063
27	BHLHE40	chr18:302234-302299	K562	blood:	n/a	n/a
28	BHLHE40	chr18:267842-268511	GM12878	blood:	n/a	chr18:268046-268062 chr18:268047-268063
29	BRCA1	chr18:267927-268244	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr18:267974-268246	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr18:267916-268222	HepG2	liver:	n/a	n/a
32	CBX3	chr18:267701-268641	K562	blood:	n/a	n/a
33	CBX3	chr18:268653-269146	K562	blood:	n/a	n/a
34	CBX3	chr18:267877-268270	K562	blood:	n/a	n/a
35	CBX3	chr18:271857-272187	K562	blood:	n/a	n/a
36	CCNT2	chr18:267628-268513	K562	blood:	n/a	n/a
37	CCNT2	chr18:306762-306890	K562	blood:	n/a	n/a
38	CEBPB	chr18:267829-268561	GM12878	blood:	n/a	n/a
39	CEBPB	chr18:267818-268289	K562	blood:	n/a	n/a
40	CEBPB	chr18:269678-269795	K562	blood:	n/a	n/a
41	CEBPB	chr18:268092-268184	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr18:269538-269869	K562	blood:	n/a	n/a
43	CEBPD	chr18:306669-307002	K562	blood:	n/a	n/a
44	CEBPD	chr18:267772-268726	K562	blood:	n/a	n/a
45	CEBPD	chr18:267595-268288	HepG2	liver:	n/a	n/a
46	CHD1	chr18:268180-268771	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr18:267960-268495	GM12878	blood:	n/a	chr18:268135-268145
48	CHD2	chr18:267902-268387	GM12878	blood:	n/a	chr18:268135-268145
49	CHD2	chr18:267876-268311	HepG2	liver:	n/a	chr18:268135-268145
50	CHD2	chr18:308135-308422	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:268256-268306	NB4	blood:	n/a
2	chr18:268256-268306	NB4	blood:	n/a
3	chr18:268166-268216	BJ	skin:	n/a
4	chr18:268256-268306	GM19239	blood:	n/a
5	chr18:268031-268081	AG09319	gingival:	n/a
6	chr18:268381-268431	PFSK-1	brain:	n/a
7	chr18:271673-271723	CMK	blood:	n/a
8	chr18:268184-268234	GM06990	blood:	n/a
9	chr18:268381-268431	Hela-S3	cervix:	n/a
10	chr18:271673-271723	HepG2	liver:	n/a
11	chr18:268601-268651	PrEC	prostate:	n/a
12	chr18:268601-268651	GM12892	blood:	n/a
13	chr18:268068-268118	GM12878	blood:	n/a
14	chr18:268184-268234	Hela-S3	cervix:	n/a
15	chr18:268381-268431	HUVEC	blood vessel:	n/a
16	chr18:268068-268118	MCF-7	breast:	n/a
17	chr18:267711-267761	HCT-116	colon:	n/a
18	chr18:268068-268118	LNCaP	prostate:	n/a
19	chr18:271673-271723	HL-60	blood:	n/a
20	chr18:268256-268306	MCF-7	breast:	n/a
21	chr18:267711-267761	AG10803	skin:	n/a
22	chr18:271673-271723	NHDF-neo	bronchial:	n/a
23	chr18:267637-267687	PrEC	prostate:	n/a
24	chr18:268068-268118	HL-60	blood:	n/a
25	chr18:268135-268185	SK-N-SH_RA	brain:	n/a
26	chr18:268381-268431	T-47D	breast:	n/a
27	chr18:268601-268651	T-47D	breast:	n/a
28	chr18:268381-268431	HMEC	breast:	n/a
29	chr18:268278-268328	AG04450	lung:	fetal
30	chr18:268131-268181	H1-hESC	embryonic stem cell:	embryo
31	chr18:268601-268651	HEK293	kidney:	embryo
32	chr18:268031-268081	NH-A	brain:	n/a
33	chr18:268256-268306	HMEC	breast:	n/a
34	chr18:268068-268118	BE2_C	brain:	n/a
35	chr18:267711-267761	AG09309	skin:	n/a
36	chr18:268166-268216	HepG2	liver:	n/a
37	chr18:268256-268306	H1-hESC	embryonic stem cell:	embryo
38	chr18:268256-268306	PANC-1	pancreas:	n/a
39	chr18:268256-268306	NHBE	bronchial:	n/a
40	chr18:268135-268185	U87	brain:	n/a
41	chr18:268135-268185	PrEC	prostate:	n/a
42	chr18:268135-268185	HIPEpiC	eye:	n/a
43	chr18:268131-268181	NHBE	bronchial:	n/a
44	chr18:268278-268328	AG04449	skin:	fetal
45	chr18:268601-268651	LNCaP	prostate:	n/a
46	chr18:268184-268234	PFSK-1	brain:	n/a
47	chr18:268184-268234	K562	blood:	n/a
48	chr18:271673-271723	SK-N-SH	brain:	n/a
49	chr18:271673-271723	HRE	kidney:	n/a
50	chr18:268166-268216	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:251595..253868-chr18:269090..271217,2	K562	blood:
2	chr18:266657..270720-chr18:273015..278448,7	MCF-7	breast:
3	chr18:302419..306527-chr18:308522..311824,4	K562	blood:
4	chr18:294145..296995-chr18:298267..301076,2	K562	blood:
5	chr18:273687..277951-chr18:283700..285982,3	K562	blood:
6	chr18:267782..268602-chr2:228189553..228190377,2	Hela-S3	cervix:
7	chr18:273244..275466-chr18:289138..290909,2	K562	blood:
8	chr18:110119..112537-chr18:266561..268595,2	MCF-7	breast:
9	chr18:263619..266135-chr18:272357..275080,2	MCF-7	breast:
10	chr18:273825..276341-chr18:276906..279543,2	K562	blood:
11	chr18:302419..306527-chr18:308522..311824,4	K562	blood:
12	chr18:267452..268053-chr9:134269416..134270075,2	Hela-S3	cervix:
13	chr18:291631..293957-chr18:611359..613782,2	MCF-7	breast:
14	chr18:251747..253552-chr18:262672..265291,2	K562	blood:
15	chr18:158336..160794-chr18:268769..270393,2	K562	blood:
16	chr18:257542..263185-chr18:266000..270349,8	MCF-7	breast:
17	chr18:286219..287016-chr18:477377..477880,2	MCF-7	breast:
18	chr18:277729..280050-chr18:615244..618128,2	MCF-7	breast:
19	chr18:254095..260758-chr18:263922..270842,11	K562	blood:
20	chr18:273600..276346-chr18:278461..281773,3	MCF-7	breast:
21	chr18:292073..293974-chr18:294604..297450,2	K562	blood:
22	chr18:269547..271961-chr18:280130..281760,2	K562	blood:
23	chr18:269653..272578-chr18:297355..299675,2	K562	blood:
24	chr18:295698..298491-chr18:306221..309182,2	MCF-7	breast:
25	chr18:292167..293133-chr18:616102..616665,2	MCF-7	breast:
26	chr18:267460..269280-chr18:657302..659143,2	MCF-7	breast:
27	chr18:250566..253483-chr18:259670..262820,3	K562	blood:
28	chr18:250537..252163-chr18:257039..259067,2	MCF-7	breast:
29	chr18:300482..306131-chr18:306212..309352,5	K562	blood:
30	chr18:273244..275466-chr18:289138..290909,2	K562	blood:
31	chr18:253259..255595-chr18:265697..268644,2	K562	blood:
32	chr18:264152..266955-chr18:267576..271730,4	MCF-7	breast:
33	chr18:286191..286695-chr18:468859..469735,2	MCF-7	breast:
34	chr18:258780..260589-chr18:262458..263959,2	MCF-7	breast:
35	chr18:295698..298491-chr18:306221..309182,2	MCF-7	breast:
36	chr18:268277..271095-chr18:349761..352127,2	K562	blood:
37	chr18:292073..293974-chr18:294604..297450,2	K562	blood:
38	chr18:249334..252987-chr18:265974..268103,4	MCF-7	breast:
39	chr18:305775..308691-chr18:309654..313982,3	K562	blood:
40	chr18:257542..263185-chr18:266000..270349,8	MCF-7	breast:
41	chr18:274502..277151-chr18:285374..288213,2	K562	blood:
42	chr18:262066..265680-chr18:266517..269152,4	MCF-7	breast:
43	chr18:269454..272332-chr18:624341..626546,2	K562	blood:
44	chr18:273600..276346-chr18:278461..281773,3	MCF-7	breast:
45	chr18:273687..277951-chr18:283700..285982,3	K562	blood:
46	chr18:226011..228697-chr18:258254..260700,2	K562	blood:
47	chr17:58235617..58237608-chr18:268202..269943,2	MCF-7	breast:
48	chr18:227929..230720-chr18:265725..267925,3	K562	blood:
49	chr18:286401..287237-chr18:477304..478254,5	MCF-7	breast:
50	chr18:269653..272578-chr18:297355..299675,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP14-3	chr18:268148-270278	ENSG00000263884.1
2	lnc-USP14-6	chr18:270815-271054	NONHSAT056835

Variant related genes	Relation type
THOC1	TF binding region
ENSG00000263884	TF binding region
ENSG00000264514	TF binding region
THOC1	CpG island
ENSG00000263884	CpG island
ENSG00000264514	CpG island
ENSG00000236432	chromatin interactions
ENSG00000176890	chromatin interactions
ENSG00000130723	chromatin interactions
ENSG00000101557	chromatin interactions
ENSG00000168958	chromatin interactions
ENSG00000176912	chromatin interactions
ENSG00000079134	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000263006	chromatin interactions
ENSG00000263884	chromatin interactions
ENSG00000079101	chromatin interactions
ENSG00000132199	chromatin interactions

Extended variants
information (count: 1960 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1960 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61752532	chr18:254315-254316	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs202031653	chr18:254368-254369	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs688526	chr18:254369-254370	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs368114729	chr18:254402-254403	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs552687695	chr18:254502-254503	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs554817221	chr18:254549-254550	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs35994127	chr18:254566-254567	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs79941676	chr18:254583-254584	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs572961998	chr18:254595-254596	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs541193806	chr18:254601-254602	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs559779759	chr18:254605-254606	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs187285437	chr18:254613-254614	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs527035	chr18:254640-254641	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs191860306	chr18:254762-254763	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs531122480	chr18:254798-254799	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs377000003	chr18:254862-254863	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs117115980	chr18:254958-254959	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs151037248	chr18:254962-254963	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs531895299	chr18:255009-255010	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs140914098	chr18:255019-255020	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs76726476	chr18:255101-255102	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs139112110	chr18:255102-255103	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs545710019	chr18:255118-255119	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs538308741	chr18:255132-255133	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs557005561	chr18:255139-255140	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs585793	chr18:255143-255144	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs114465542	chr18:255156-255157	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs142827149	chr18:255194-255195	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs146981592	chr18:255209-255210	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs540414368	chr18:255210-255211	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs138112967	chr18:255259-255260	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs578053750	chr18:255268-255269	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs545063015	chr18:255305-255306	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs530274078	chr18:255306-255307	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs371593663	chr18:255336-255337	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs563358392	chr18:255341-255342	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs530786811	chr18:255387-255388	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs542943856	chr18:255429-255430	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs561612808	chr18:255444-255445	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs117810759	chr18:255451-255452	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs547174485	chr18:255479-255480	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs149537963	chr18:255499-255500	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs532161287	chr18:255535-255536	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs500596	chr18:255552-255553	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs144103621	chr18:255581-255582	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs78118502	chr18:255622-255623	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs7506417	chr18:255741-255742	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs182485587	chr18:255769-255770	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs532417070	chr18:255783-255784	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs566757606	chr18:255799-255800	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Esophageal cancer	21851588	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Breast cancer	17899364	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Gastrointestinal cancer	17018589	CNVD
prenatal diagnosis	20453657	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Renal cell carcinoma	18765545	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Melanoma	17363583	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	20808228	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
Cancer	20164919	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	21865298	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:1117 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:212000-256400	Weak transcription	Gastric	stomach
2	chr18:218000-267400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr18:218600-261400	Weak transcription	Pancreas	Pancrea
4	chr18:218600-267200	Weak transcription	Stomach Mucosa	stomach
5	chr18:219000-267200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr18:219000-267200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr18:225200-254600	Weak transcription	Right Ventricle	heart
8	chr18:238000-265800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
9	chr18:238000-266200	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr18:238200-265000	Strong transcription	Primary T helper cells PMA-I stimulated	--
11	chr18:238400-265800	Strong transcription	HUES48 Cell Line	embryonic stem cell
12	chr18:239600-258200	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr18:239600-265200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr18:239600-265200	Strong transcription	Liver	Liver
15	chr18:239800-265800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
16	chr18:240000-265200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr18:240200-265200	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr18:240200-265200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
19	chr18:240200-265400	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr18:240600-255400	Weak transcription	Fetal Heart	heart
21	chr18:240600-258600	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr18:240600-266200	Strong transcription	Primary B cells from cord blood	blood
23	chr18:241000-260800	Strong transcription	Primary B cells from peripheral blood	blood
24	chr18:241200-265400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr18:241400-259800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr18:241600-255000	Weak transcription	Spleen	Spleen
27	chr18:241600-259400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr18:241600-261400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr18:241600-265600	Strong transcription	Fetal Thymus	thymus
30	chr18:242600-260000	Strong transcription	Skeletal Muscle Female	skeletal muscle
31	chr18:243000-262200	Strong transcription	HepG2	liver
32	chr18:243200-265600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr18:243600-265000	Strong transcription	Adipose Nuclei	Adipose
34	chr18:243800-262000	Strong transcription	HSMM	muscle
35	chr18:243800-265600	Strong transcription	Fetal Intestine Large	intestine
36	chr18:244200-260400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr18:244200-265600	Strong transcription	Dnd41	blood
38	chr18:244400-259800	Strong transcription	H1 Cell Line	embryonic stem cell
39	chr18:244400-259800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr18:244400-265000	Strong transcription	Rectal Mucosa Donor 29	rectum
41	chr18:244400-265400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr18:244400-265400	Strong transcription	Placenta	Placenta
43	chr18:244600-257400	Strong transcription	Duodenum Smooth Muscle	Duodenum
44	chr18:244600-265000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr18:245000-265800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr18:245200-265800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr18:245400-266200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr18:245800-255000	Weak transcription	Rectal Smooth Muscle	rectum
49	chr18:245800-266000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr18:245800-267400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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