Variant report

Variant	esv2763339
Chromosome Location	chr4:9858426-10056376
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3269)
CpG islands
(count:1892)
Chromatin interactive
region (count:75)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3269 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:9998163-9998719	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:10009929-10010129	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:9965207-9965232	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:10007887-10008235	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:10020424-10020705	K562	blood:	n/a	n/a
6	ARID3A	chr4:10004013-10004296	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:10018550-10019341	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:10046913-10047474	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:10032742-10033066	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:10027037-10027405	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:10013565-10013836	K562	blood:	n/a	n/a
12	ARID3A	chr4:10023038-10023398	HepG2	liver:	n/a	n/a
13	ARID3A	chr4:9952887-9953127	K562	blood:	n/a	n/a
14	ARID3A	chr4:10008544-10008869	HepG2	liver:	n/a	n/a
15	ARID3A	chr4:10048100-10048213	HepG2	liver:	n/a	n/a
16	ATF1	chr4:9927280-9927595	K562	blood:	n/a	n/a
17	ATF1	chr4:10025316-10025600	K562	blood:	n/a	n/a
18	ATF1	chr4:9929162-9929613	K562	blood:	n/a	n/a
19	ATF1	chr4:10011611-10011843	K562	blood:	n/a	n/a
20	ATF1	chr4:10013493-10013865	K562	blood:	n/a	n/a
21	ATF2	chr4:9972118-9972587	GM12878	blood:	n/a	n/a
22	ATF2	chr4:10008476-10009984	GM12878	blood:	n/a	n/a
23	ATF2	chr4:10007851-10008196	GM12878	blood:	n/a	n/a
24	ATF2	chr4:10001424-10002312	GM12878	blood:	n/a	n/a
25	ATF2	chr4:10020411-10021134	GM12878	blood:	n/a	n/a
26	ATF2	chr4:10001436-10002278	GM12878	blood:	n/a	n/a
27	ATF2	chr4:10007760-10008278	GM12878	blood:	n/a	n/a
28	ATF2	chr4:10008534-10009956	GM12878	blood:	n/a	n/a
29	ATF2	chr4:9991905-9992354	GM12878	blood:	n/a	n/a
30	ATF2	chr4:10005306-10005725	GM12878	blood:	n/a	n/a
31	ATF2	chr4:10020339-10020818	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF3	chr4:10020397-10020713	K562	blood:	n/a	n/a
33	ATF3	chr4:10003452-10003631	K562	blood:	n/a	n/a
34	ATF3	chr4:10020471-10020640	GM12878	blood:	n/a	n/a
35	ATF3	chr4:10020361-10020755	H1-hESC	embryonic stem cell:	n/a	n/a
36	ATF3	chr4:10013615-10013860	K562	blood:	n/a	n/a
37	ATF3	chr4:10034340-10034597	K562	blood:	n/a	chr4:10034394-10034408
38	BACH1	chr4:9885168-9885286	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr4:10028131-10028378	K562	blood:	n/a	n/a
40	BACH1	chr4:10034449-10034649	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr4:10020394-10020795	H1-hESC	embryonic stem cell:	n/a	n/a
42	BATF	chr4:10025493-10025778	GM12878	blood:	n/a	chr4:10025549-10025562 chr4:10025631-10025642
43	BATF	chr4:10020385-10020681	GM12878	blood:	n/a	n/a
44	BATF	chr4:10009240-10009722	GM12878	blood:	n/a	n/a
45	BATF	chr4:10008580-10009742	GM12878	blood:	n/a	chr4:10009169-10009177
46	BATF	chr4:10005411-10005658	GM12878	blood:	n/a	chr4:10005512-10005523
47	BATF	chr4:10001742-10002251	GM12878	blood:	n/a	n/a
48	BATF	chr4:9972302-9972703	GM12878	blood:	n/a	n/a
49	BCL11A	chr4:9972269-9972776	GM12878	blood:	n/a	n/a
50	BCL11A	chr4:10008840-10009820	GM12878	blood:	n/a	chr4:10009092-10009101

(count:1892 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10042842-10042892	GM12878	blood:	n/a
2	chr4:10042842-10042892	GM12878	blood:	n/a
3	chr4:10022984-10023034	AG04449	skin:	fetal
4	chr4:10042449-10042499	K562	blood:	n/a
5	chr4:10042842-10042892	HCPEpiC	choroid plexus:	n/a
6	chr4:10041000-10041050	PFSK-1	brain:	n/a
7	chr4:9990048-9990098	AG09309	skin:	n/a
8	chr4:10042198-10042248	U87	brain:	n/a
9	chr4:10020555-10020605	HRE	kidney:	n/a
10	chr4:10020555-10020605	HepG2	liver:	n/a
11	chr4:10042842-10042892	HRE	kidney:	n/a
12	chr4:9937674-9937724	BE2_C	brain:	n/a
13	chr4:9998017-9998067	SAEC	small airway:	n/a
14	chr4:9990048-9990098	A549	lung:	n/a
15	chr4:10020634-10020684	T-47D	breast:	n/a
16	chr4:9990048-9990098	NT2-D1	testis:	n/a
17	chr4:9922462-9922512	GM19239	blood:	n/a
18	chr4:9884128-9884178	ProgFib	skin:	n/a
19	chr4:10021025-10021075	AG04449	skin:	fetal
20	chr4:9990048-9990098	HRPEpiC	eye:	n/a
21	chr4:10041776-10041826	HRCEpiC	kidney:	n/a
22	chr4:9892887-9892937	HIPEpiC	eye:	n/a
23	chr4:10019009-10019059	ECC-1	luminal epithelium:	n/a
24	chr4:10024364-10024414	BE2_C	brain:	n/a
25	chr4:10041000-10041050	HEEpiC	esophagus:	n/a
26	chr4:10041776-10041826	Hepatocyte	liver:	n/a
27	chr4:10020882-10020932	HRE	kidney:	n/a
28	chr4:10019009-10019059	BE2_C	brain:	n/a
29	chr4:10020634-10020684	ovcar-3	ovarian:	n/a
30	chr4:10009916-10009966	HIPEpiC	eye:	n/a
31	chr4:9950643-9950693	RPTEC	kidney:	n/a
32	chr4:10034580-10034630	AG09319	gingival:	n/a
33	chr4:10019009-10019059	NB4	blood:	n/a
34	chr4:9922462-9922512	Jurkat	blood:	n/a
35	chr4:9940566-9940616	HCT-116	colon:	n/a
36	chr4:10020360-10020410	AG09319	gingival:	n/a
37	chr4:10016908-10016958	HCPEpiC	choroid plexus:	n/a
38	chr4:10041000-10041050	SK-N-MC	brain:	n/a
39	chr4:10021025-10021075	AG10803	skin:	n/a
40	chr4:9937674-9937724	NH-A	brain:	n/a
41	chr4:9990048-9990098	NHBE	bronchial:	n/a
42	chr4:9917839-9917889	RPTEC	kidney:	n/a
43	chr4:10034580-10034630	ovcar-3	ovarian:	n/a
44	chr4:10042198-10042248	RPTEC	kidney:	n/a
45	chr4:10021025-10021075	AoSMC	blood vessel:	n/a
46	chr4:9937674-9937724	PANC-1	pancreas:	n/a
47	chr4:9950643-9950693	BJ	skin:	n/a
48	chr4:9981202-9981252	NB4	blood:	n/a
49	chr4:9940566-9940616	AG09309	skin:	n/a
50	chr4:10020634-10020684	CMK	blood:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:9766226..9767390-chr4:9899951..9901032,8	MCF-7	breast:
2	chr4:10003454..10005588-chr4:10009688..10011673,2	MCF-7	breast:
3	chr4:9898528..9900449-chr4:10019179..10021130,2	MCF-7	breast:
4	chr4:9764428..9765300-chr4:10016550..10017565,3	K562	blood:
5	chr4:10050227..10052553-chr4:10054498..10056882,2	K562	blood:
6	chr4:10007258..10010277-chr4:10010409..10012241,3	MCF-7	breast:
7	chr4:10015413..10017936-chr4:10018958..10020655,2	MCF-7	breast:
8	chr4:9903730..9906582-chr4:9912941..9915065,2	MCF-7	breast:
9	chr4:10028896..10030894-chr4:10122706..10125313,2	K562	blood:
10	chr4:10008558..10010473-chr4:10063451..10065782,2	MCF-7	breast:
11	chr4:9869830..9872812-chr4:9880250..9882960,2	K562	blood:
12	chr4:9770192..9773137-chr4:10024212..10026749,2	K562	blood:
13	chr4:10008545..10009273-chr4:10020464..10021005,2	MCF-7	breast:
14	chr4:10033030..10034868-chr4:10118461..10119964,2	MCF-7	breast:
15	chr4:9920609..9921128-chr4:10020066..10020974,2	K562	blood:
16	chr4:9931454..9932279-chr4:10015120..10015668,2	MCF-7	breast:
17	chr4:10009870..10011594-chr4:10018076..10020950,2	MCF-7	breast:
18	chr4:9999925..10002392-chr4:10005670..10008448,2	K562	blood:
19	chr4:9924672..9926796-chr4:10008145..10009788,2	MCF-7	breast:
20	chr4:10032509..10034533-chr4:10096806..10099727,2	K562	blood:
21	chr4:9865151..9867306-chr4:9868074..9870913,3	MCF-7	breast:
22	chr4:10019361..10022054-chr4:10108000..10110178,2	K562	blood:
23	chr4:10014497..10017156-chr4:10035550..10037272,2	K562	blood:
24	chr4:9766848..9767385-chr4:9900038..9900893,4	MCF-7	breast:
25	chr4:9764793..9765717-chr4:10015113..10016017,3	MCF-7	breast:
26	chr4:9865151..9867306-chr4:9868074..9870913,3	MCF-7	breast:
27	chr4:10013756..10016342-chr4:10019504..10023873,3	K562	blood:
28	chr4:9999663..10002309-chr4:10003898..10006601,3	MCF-7	breast:
29	chr4:9903730..9906582-chr4:9912941..9915065,2	MCF-7	breast:
30	chr4:9763456..9766236-chr4:10014004..10016919,3	K562	blood:
31	chr4:9999663..10002309-chr4:10003898..10006601,3	MCF-7	breast:
32	chr4:10008851..10011783-chr4:10012924..10016004,5	MCF-7	breast:
33	chr4:9764370..9765339-chr4:10015197..10016013,4	MCF-7	breast:
34	chr4:10008415..10010213-chr4:10011796..10014245,2	K562	blood:
35	chr4:9931197..9931753-chr4:10016553..10017073,2	MCF-7	breast:
36	chr4:10008415..10010213-chr4:10011796..10014245,2	K562	blood:
37	chr4:10019661..10022849-chr4:10023062..10025452,3	K562	blood:
38	chr4:9957351..9959521-chr4:10008550..10011275,2	MCF-7	breast:
39	chr4:9931197..9931753-chr4:10016553..10017073,2	MCF-7	breast:
40	chr4:9959731..9961810-chr4:9971031..9973164,2	K562	blood:
41	chr4:9764792..9765537-chr4:9899989..9900954,5	MCF-7	breast:
42	chr4:9929005..9929948-chr4:10015148..10015863,2	MCF-7	breast:
43	chr4:10053096..10055486-chr4:10058375..10060110,2	K562	blood:
44	chr4:9957351..9959521-chr4:10008550..10011275,2	MCF-7	breast:
45	chr4:9764417..9765133-chr4:10016121..10017439,5	MCF-7	breast:
46	chr4:10031896..10034212-chr4:10409451..10411616,2	K562	blood:
47	chr4:10020536..10023325-chr4:10025799..10029050,4	K562	blood:
48	chr4:10031202..10033907-chr4:10037747..10039900,2	K562	blood:
49	chr4:10020691..10022205-chr4:10031735..10034033,2	K562	blood:
50	chr4:10020622..10022306-chr4:10022841..10025006,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DRD5-1	chr4:9925400-9925770	ENSG00000249219.1
2	lnc-WDR1-12	chr4:9870401-9871383	NONHSAT095146
3	lnc-WDR1-3	chr4:10035849-10037764	NONHSAT095153
4	lnc-WDR1-12	chr4:9873428-9874487	NONHSAT095146
5	lnc-DRD5-1	chr4:9924438-9924574	ENSG00000249219.1
6	lnc-WDR1-3	chr4:10041754-10042012	NONHSAT095153
7	lnc-WDR1-3	chr4:10035858-10036380	NONHSAT095155
8	lnc-WDR1-3	chr4:10035858-10036286	NONHSAT095154
9	lnc-WDR1-3	chr4:10036546-10037004	NONHSAT095155
10	lnc-DRD5-2	chr4:10011102-10011349	ENSG00000250413.1
11	lnc-WDR1-3	chr4:10036546-10037004	NONHSAT095154
12	lnc-WDR1-5	chr4:10027348-10027630	NONHSAT095152
13	lnc-DRD5-2	chr4:10008106-10008316	ENSG00000250413.1
14	lnc-WDR1-5	chr4:10030642-10030924	NONHSAT095152

No data

Variant related genes	Relation type
ENSG00000250413	TF binding region
ENSG00000249219	TF binding region
SLC2A9	TF binding region
ENSG00000250413	CpG island
ENSG00000249219	CpG island
SLC2A9	CpG island
ENSG00000071127	chromatin interactions
ENSG00000109667	chromatin interactions
ENSG00000264931	chromatin interactions
ENSG00000250413	chromatin interactions
ENSG00000223086	chromatin interactions

Extended variants
information (count: 8843 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:8843 , 50 per page) page: 1 2 3 4 5 6 7 ... 177

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56014085	chr4:9858457-9858458	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552665125	chr4:9858468-9858469	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538044264	chr4:9858482-9858483	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs4697691	chr4:9858485-9858486	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs140141642	chr4:9858536-9858537	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375476641	chr4:9858547-9858548	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs190229873	chr4:9858548-9858549	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569896513	chr4:9858553-9858554	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs536955428	chr4:9858561-9858562	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561419851	chr4:9858575-9858576	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572879366	chr4:9858582-9858583	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192114242	chr4:9858603-9858604	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184245647	chr4:9858643-9858644	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs11728377	chr4:9858701-9858702	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs544750647	chr4:9858718-9858719	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562956439	chr4:9858727-9858728	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs4575993	chr4:9858744-9858745	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs551481241	chr4:9858758-9858759	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560325301	chr4:9858763-9858764	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146954929	chr4:9858783-9858784	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548753086	chr4:9858820-9858821	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567508379	chr4:9858825-9858826	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540660092	chr4:9858831-9858832	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537756937	chr4:9858834-9858835	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188615982	chr4:9858842-9858843	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549911920	chr4:9858876-9858877	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138041093	chr4:9858956-9858957	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553012085	chr4:9858957-9858958	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538472063	chr4:9858963-9858964	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141720595	chr4:9858984-9858985	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566663391	chr4:9858985-9858986	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546163823	chr4:9859047-9859048	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534194343	chr4:9859052-9859053	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374149140	chr4:9859074-9859075	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574241277	chr4:9859107-9859108	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs77387738	chr4:9859112-9859113	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181315906	chr4:9859141-9859142	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs578207088	chr4:9859152-9859153	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545660436	chr4:9859156-9859157	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs61209374	chr4:9859160-9859161	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs527401789	chr4:9859165-9859166	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542565981	chr4:9859167-9859168	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560734223	chr4:9859187-9859188	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375506452	chr4:9859191-9859192	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531603096	chr4:9859224-9859225	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561335769	chr4:9859391-9859392	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115536550	chr4:9859423-9859424	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571240724	chr4:9859478-9859479	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs56970526	chr4:9859557-9859558	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs547235115	chr4:9859571-9859572	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
early-passage human iPS cells	21368824	CNVD
Sinonasal adenocarcinoma	21360264	CNVD
Breast cancer	17142309	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2809 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9845000-9874800	Weak transcription	NHEK	skin
2	chr4:9848600-9861800	Weak transcription	HMEC	breast
3	chr4:9850200-9858800	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr4:9851200-9869800	Weak transcription	Gastric	stomach
5	chr4:9851400-9859000	Weak transcription	HepG2	liver
6	chr4:9852400-9858800	Weak transcription	Fetal Intestine Small	intestine
7	chr4:9853200-9858800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr4:9856800-9861200	Weak transcription	Liver	Liver
9	chr4:9857200-9864800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:9858000-9862800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
11	chr4:9858200-9859600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr4:9858200-9861800	Weak transcription	Fetal Intestine Large	intestine
13	chr4:9858400-9867000	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr4:9858800-9859400	Strong transcription	Fetal Intestine Small	intestine
15	chr4:9858800-9859600	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
16	chr4:9858800-9863200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr4:9859000-9859400	Strong transcription	HepG2	liver
18	chr4:9859400-9861400	Weak transcription	Fetal Intestine Small	intestine
19	chr4:9859400-9861600	Weak transcription	HepG2	liver
20	chr4:9859600-9861200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr4:9859600-9861400	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr4:9859800-9862600	Weak transcription	Small Intestine	intestine
23	chr4:9860200-9861800	Weak transcription	Duodenum Mucosa	Duodenum
24	chr4:9861000-9864800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr4:9861200-9863400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:9861200-9863600	Strong transcription	Liver	Liver
27	chr4:9861400-9862600	Strong transcription	Fetal Intestine Small	intestine
28	chr4:9861400-9864400	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr4:9861600-9861800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr4:9861600-9862000	ZNF genes & repeats	Brain Hippocampus Middle	brain
31	chr4:9861600-9862600	ZNF genes & repeats	Aorta	Aorta
32	chr4:9861600-9863800	Weak transcription	Right Ventricle	heart
33	chr4:9861600-9864400	Strong transcription	HepG2	liver
34	chr4:9861600-9874400	Weak transcription	Stomach Smooth Muscle	stomach
35	chr4:9861800-9862200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
36	chr4:9861800-9862400	ZNF genes & repeats	Pancreas	Pancrea
37	chr4:9861800-9862600	ZNF genes & repeats	Adipose Nuclei	Adipose
38	chr4:9861800-9862600	ZNF genes & repeats	Esophagus	oesophagus
39	chr4:9861800-9862600	Strong transcription	HMEC	breast
40	chr4:9861800-9862800	Strong transcription	Duodenum Mucosa	Duodenum
41	chr4:9861800-9862800	Strong transcription	Fetal Intestine Large	intestine
42	chr4:9861800-9864200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr4:9862000-9862600	ZNF genes & repeats	Lung	lung
44	chr4:9862200-9862600	Strong transcription	Duodenum Smooth Muscle	Duodenum
45	chr4:9862600-9863000	Weak transcription	Adipose Nuclei	Adipose
46	chr4:9862600-9863600	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr4:9862600-9868200	Weak transcription	Lung	lung
48	chr4:9862600-9871600	Weak transcription	Fetal Intestine Small	intestine
49	chr4:9862600-9880400	Weak transcription	HMEC	breast
50	chr4:9862600-9883000	Weak transcription	Esophagus	oesophagus

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