Variant report

Variant	nsv878688
Chromosome Location	chr4:9915850-10038112
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2632)
CpG islands
(count:1404)
Chromatin interactive
region (count:61)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2632 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:10008544-10008869	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:10004013-10004296	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:9965207-9965232	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:10032742-10033066	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:10023038-10023398	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:9952887-9953127	K562	blood:	n/a	n/a
7	ARID3A	chr4:10009929-10010129	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:10013565-10013836	K562	blood:	n/a	n/a
9	ARID3A	chr4:10018550-10019341	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:9998163-9998719	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:10007887-10008235	HepG2	liver:	n/a	n/a
12	ARID3A	chr4:10020424-10020705	K562	blood:	n/a	n/a
13	ARID3A	chr4:10027037-10027405	HepG2	liver:	n/a	n/a
14	ATF1	chr4:9927280-9927595	K562	blood:	n/a	n/a
15	ATF1	chr4:10011611-10011843	K562	blood:	n/a	n/a
16	ATF1	chr4:10025316-10025600	K562	blood:	n/a	n/a
17	ATF1	chr4:10013493-10013865	K562	blood:	n/a	n/a
18	ATF1	chr4:9929162-9929613	K562	blood:	n/a	n/a
19	ATF2	chr4:10020339-10020818	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr4:9972118-9972587	GM12878	blood:	n/a	n/a
21	ATF2	chr4:10005306-10005725	GM12878	blood:	n/a	n/a
22	ATF2	chr4:10020411-10021134	GM12878	blood:	n/a	n/a
23	ATF2	chr4:10008534-10009956	GM12878	blood:	n/a	n/a
24	ATF2	chr4:10001436-10002278	GM12878	blood:	n/a	n/a
25	ATF2	chr4:10007760-10008278	GM12878	blood:	n/a	n/a
26	ATF2	chr4:10007851-10008196	GM12878	blood:	n/a	n/a
27	ATF2	chr4:10001424-10002312	GM12878	blood:	n/a	n/a
28	ATF2	chr4:10008476-10009984	GM12878	blood:	n/a	n/a
29	ATF2	chr4:9991905-9992354	GM12878	blood:	n/a	n/a
30	ATF3	chr4:10020471-10020640	GM12878	blood:	n/a	n/a
31	ATF3	chr4:10003452-10003631	K562	blood:	n/a	n/a
32	ATF3	chr4:10013615-10013860	K562	blood:	n/a	n/a
33	ATF3	chr4:10020397-10020713	K562	blood:	n/a	n/a
34	ATF3	chr4:10034340-10034597	K562	blood:	n/a	chr4:10034394-10034408
35	ATF3	chr4:10020361-10020755	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr4:10028131-10028378	K562	blood:	n/a	n/a
37	BACH1	chr4:10020394-10020795	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr4:10034449-10034649	H1-hESC	embryonic stem cell:	n/a	n/a
39	BATF	chr4:10025493-10025778	GM12878	blood:	n/a	chr4:10025549-10025562 chr4:10025631-10025642
40	BATF	chr4:10005411-10005658	GM12878	blood:	n/a	chr4:10005512-10005523
41	BATF	chr4:10008580-10009742	GM12878	blood:	n/a	chr4:10009169-10009177
42	BATF	chr4:9972302-9972703	GM12878	blood:	n/a	n/a
43	BATF	chr4:10001742-10002251	GM12878	blood:	n/a	n/a
44	BATF	chr4:10020385-10020681	GM12878	blood:	n/a	n/a
45	BATF	chr4:10009240-10009722	GM12878	blood:	n/a	n/a
46	BCL11A	chr4:9972269-9972776	GM12878	blood:	n/a	n/a
47	BCL11A	chr4:10008802-10009231	GM12878	blood:	n/a	chr4:10009092-10009101
48	BCL11A	chr4:10009303-10009699	GM12878	blood:	n/a	n/a
49	BCL11A	chr4:10008840-10009820	GM12878	blood:	n/a	chr4:10009092-10009101
50	BCL11A	chr4:9972312-9972693	GM12878	blood:	n/a	n/a

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10016908-10016958	SKMC	muscle:	n/a
2	chr4:10016908-10016958	SKMC	muscle:	n/a
3	chr4:10020360-10020410	AG09309	skin:	n/a
4	chr4:9926439-9926489	HPAEpiC	pulmonary alveolar:	n/a
5	chr4:9990048-9990098	SK-N-MC	brain:	n/a
6	chr4:10023201-10023251	HNPCEpiC	eye:	n/a
7	chr4:10024364-10024414	AoSMC	blood vessel:	n/a
8	chr4:10034580-10034630	HAEpiC	amniotic membrane:	n/a
9	chr4:9937674-9937724	T-47D	breast:	n/a
10	chr4:10023201-10023251	NB4	blood:	n/a
11	chr4:10024412-10024462	BE2_C	brain:	n/a
12	chr4:9990048-9990098	HRE	kidney:	n/a
13	chr4:10020634-10020684	AoSMC	blood vessel:	n/a
14	chr4:9990048-9990098	T-47D	breast:	n/a
15	chr4:10020360-10020410	AG04449	skin:	fetal
16	chr4:10022984-10023034	MCF-7	breast:	n/a
17	chr4:9922462-9922512	T-47D	breast:	n/a
18	chr4:9950643-9950693	NT2-D1	testis:	n/a
19	chr4:9917839-9917889	PFSK-1	brain:	n/a
20	chr4:10019009-10019059	BJ	skin:	n/a
21	chr4:10024412-10024462	T-47D	breast:	n/a
22	chr4:10016908-10016958	ECC-1	luminal epithelium:	n/a
23	chr4:9998017-9998067	CMK	blood:	n/a
24	chr4:9990048-9990098	ProgFib	skin:	n/a
25	chr4:9937674-9937724	HepG2	liver:	n/a
26	chr4:9950643-9950693	AG04450	lung:	fetal
27	chr4:9926439-9926489	HCM	heart:	n/a
28	chr4:9981202-9981252	Caco-2	colon:	n/a
29	chr4:10009916-10009966	GM12891	blood:	n/a
30	chr4:10020360-10020410	Hepatocyte	liver:	n/a
31	chr4:9922462-9922512	A549	lung:	n/a
32	chr4:10019009-10019059	PANC-1	pancreas:	n/a
33	chr4:10022984-10023034	NH-A	brain:	n/a
34	chr4:10024364-10024414	PrEC	prostate:	n/a
35	chr4:10019009-10019059	HRE	kidney:	n/a
36	chr4:9990048-9990098	MCF-7	breast:	n/a
37	chr4:9990048-9990098	AG09309	skin:	n/a
38	chr4:10021355-10021405	SAEC	small airway:	n/a
39	chr4:10023201-10023251	HRCEpiC	kidney:	n/a
40	chr4:9950643-9950693	AG09319	gingival:	n/a
41	chr4:9990048-9990098	H1-hESC	embryonic stem cell:	embryo
42	chr4:9937674-9937724	CMK	blood:	n/a
43	chr4:10020882-10020932	HCF	heart:	n/a
44	chr4:10022984-10023034	Hela-S3	cervix:	n/a
45	chr4:9926439-9926489	SK-N-SH_RA	brain:	n/a
46	chr4:10019009-10019059	NHBE	bronchial:	n/a
47	chr4:10020360-10020410	T-47D	breast:	n/a
48	chr4:10020634-10020684	U87	brain:	n/a
49	chr4:9937674-9937724	HUVEC	blood vessel:	n/a
50	chr4:10009916-10009966	SAEC	small airway:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:9931454..9932279-chr4:10015120..10015668,2	MCF-7	breast:
2	chr4:9764370..9765339-chr4:10015197..10016013,4	MCF-7	breast:
3	chr4:10031896..10034212-chr4:10409451..10411616,2	K562	blood:
4	chr4:10014545..10016342-chr4:10019504..10022397,2	K562	blood:
5	chr4:9929005..9929948-chr4:10015148..10015863,2	MCF-7	breast:
6	chr4:10003454..10005588-chr4:10009688..10011673,2	MCF-7	breast:
7	chr4:9764417..9765133-chr4:10016121..10017439,5	MCF-7	breast:
8	chr4:10028896..10030894-chr4:10122706..10125313,2	K562	blood:
9	chr4:9920436..9923282-chr4:9925910..9928355,2	MCF-7	breast:
10	chr4:10013756..10016342-chr4:10019504..10023873,3	K562	blood:
11	chr4:9918331..9921142-chr4:10116868..10118418,2	MCF-7	breast:
12	chr4:9920436..9923282-chr4:9925910..9928355,2	MCF-7	breast:
13	chr4:10019661..10022849-chr4:10023062..10025452,3	K562	blood:
14	chr4:10008545..10009273-chr4:10020464..10021005,2	MCF-7	breast:
15	chr4:9704873..9705750-chr4:10016280..10017221,3	K562	blood:
16	chr4:10019661..10022849-chr4:10023062..10025452,3	K562	blood:
17	chr4:9999663..10002309-chr4:10003898..10006601,3	MCF-7	breast:
18	chr4:10008851..10011783-chr4:10012924..10016004,5	MCF-7	breast:
19	chr4:9764428..9765300-chr4:10016550..10017565,3	K562	blood:
20	chr4:9931454..9932279-chr4:10015120..10015668,2	MCF-7	breast:
21	chr4:9764866..9765415-chr4:9928949..9929492,2	MCF-7	breast:
22	chr4:10003454..10005588-chr4:10009688..10011673,2	MCF-7	breast:
23	chr4:9761130..9763005-chr4:9988480..9990175,2	K562	blood:
24	chr4:10032509..10034533-chr4:10096806..10099727,2	K562	blood:
25	chr4:9957351..9959521-chr4:10008550..10011275,2	MCF-7	breast:
26	chr4:10008415..10010213-chr4:10011796..10014245,2	K562	blood:
27	chr4:10020691..10022205-chr4:10031735..10034033,2	K562	blood:
28	chr4:10020627..10022375-chr4:10032476..10035233,2	K562	blood:
29	chr4:10031202..10033907-chr4:10037747..10039900,2	K562	blood:
30	chr4:10008415..10010213-chr4:10011796..10014245,2	K562	blood:
31	chr4:10020536..10023325-chr4:10025799..10029050,4	K562	blood:
32	chr4:9763456..9766236-chr4:10014004..10016919,3	K562	blood:
33	chr4:10009870..10011594-chr4:10018076..10020950,2	MCF-7	breast:
34	chr4:10019361..10022054-chr4:10108000..10110178,2	K562	blood:
35	chr4:10031202..10033907-chr4:10037747..10039900,2	K562	blood:
36	chr4:10014497..10017156-chr4:10035550..10037272,2	K562	blood:
37	chr4:9957351..9959521-chr4:10008550..10011275,2	MCF-7	breast:
38	chr4:10015413..10017936-chr4:10018958..10020655,2	MCF-7	breast:
39	chr4:10007258..10010277-chr4:10010409..10012241,3	MCF-7	breast:
40	chr4:9770192..9773137-chr4:10024212..10026749,2	K562	blood:
41	chr4:10020622..10022306-chr4:10022841..10025006,2	MCF-7	breast:
42	chr4:9931197..9931753-chr4:10016553..10017073,2	MCF-7	breast:
43	chr4:9999925..10002392-chr4:10005670..10008448,2	K562	blood:
44	chr4:10014497..10017156-chr4:10035550..10037272,2	K562	blood:
45	chr4:9704779..9705714-chr4:10015117..10016069,5	MCF-7	breast:
46	chr4:9764793..9765717-chr4:10015113..10016017,3	MCF-7	breast:
47	chr4:9924672..9926796-chr4:10008145..10009788,2	MCF-7	breast:
48	chr4:9766485..9767197-chr4:10016698..10017481,2	MCF-7	breast:
49	chr4:10008717..10011087-chr4:10117692..10120073,3	MCF-7	breast:
50	chr4:9999663..10002309-chr4:10003898..10006601,3	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR1-3	chr4:10036546-10037004	NONHSAT095155
2	lnc-WDR1-3	chr4:10035858-10036286	NONHSAT095154
3	lnc-DRD5-1	chr4:9924438-9924574	ENSG00000249219.1
4	lnc-WDR1-3	chr4:10035858-10036380	NONHSAT095155
5	lnc-WDR1-5	chr4:10030642-10030924	NONHSAT095152
6	lnc-DRD5-1	chr4:9925400-9925770	ENSG00000249219.1
7	lnc-DRD5-2	chr4:10011102-10011349	ENSG00000250413.1
8	lnc-WDR1-3	chr4:10036546-10037004	NONHSAT095154
9	lnc-WDR1-3	chr4:10035849-10037764	NONHSAT095153
10	lnc-DRD5-2	chr4:10008106-10008316	ENSG00000250413.1
11	lnc-WDR1-5	chr4:10027348-10027630	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
ENSG00000223086	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000250413	chromatin interactions
ENSG00000109667	chromatin interactions

Extended variants
information (count: 5466 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5466 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4697695	chr4:9915850-9915851	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs79656154	chr4:9915856-9915857	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560162229	chr4:9915866-9915867	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs4697696	chr4:9915870-9915871	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs386671556	chr4:9915872-9915873	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs4697697	chr4:9915874-9915875	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs192898819	chr4:9915895-9915896	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550124862	chr4:9915908-9915909	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375094968	chr4:9915952-9915953	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs538743156	chr4:9915961-9915962	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547404816	chr4:9915982-9915983	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183301004	chr4:9915998-9915999	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536526759	chr4:9916004-9916005	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs112558516	chr4:9916089-9916090	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs116881794	chr4:9916113-9916114	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537208314	chr4:9916126-9916127	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558475262	chr4:9916127-9916128	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75181558	chr4:9916133-9916134	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370598574	chr4:9916145-9916146	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187792511	chr4:9916146-9916147	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs7674711	chr4:9916180-9916181	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs147336879	chr4:9916187-9916188	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148295578	chr4:9916194-9916195	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561595181	chr4:9916201-9916202	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7674723	chr4:9916202-9916203	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs74433158	chr4:9916206-9916207	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10516194	chr4:9916209-9916210	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs578204542	chr4:9916230-9916231	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545374613	chr4:9916247-9916248	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547540981	chr4:9916282-9916283	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs115224046	chr4:9916318-9916319	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191513628	chr4:9916332-9916333	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs114108333	chr4:9916337-9916338	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569884068	chr4:9916342-9916343	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569205867	chr4:9916343-9916344	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs116576416	chr4:9916367-9916368	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79419742	chr4:9916426-9916427	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570590218	chr4:9916432-9916433	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs115603911	chr4:9916436-9916437	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188216363	chr4:9916476-9916477	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78301913	chr4:9916574-9916575	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs73094597	chr4:9916593-9916594	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192598731	chr4:9916595-9916596	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76856001	chr4:9916640-9916641	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543793930	chr4:9916649-9916650	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs16890905	chr4:9916662-9916663	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs532722835	chr4:9916664-9916665	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139310234	chr4:9916679-9916680	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs142509857	chr4:9916682-9916683	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561455175	chr4:9916712-9916713	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
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

Chromatin state (count:2215 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9894000-9917800	Weak transcription	Lung	lung
2	chr4:9897000-9924600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
3	chr4:9903400-9923200	Strong transcription	HepG2	liver
4	chr4:9903600-9916000	Strong transcription	Fetal Intestine Large	intestine
5	chr4:9903600-9928600	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr4:9903600-9929000	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr4:9907000-9918400	Weak transcription	Left Ventricle	heart
8	chr4:9907200-9919400	Weak transcription	Esophagus	oesophagus
9	chr4:9907400-9916600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr4:9907400-9923200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr4:9908000-9943000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr4:9911000-9916600	Strong transcription	NHEK	skin
13	chr4:9911400-9916000	Weak transcription	Liver	Liver
14	chr4:9911400-9919400	Weak transcription	Aorta	Aorta
15	chr4:9911400-9920200	Weak transcription	Stomach Smooth Muscle	stomach
16	chr4:9911400-9979800	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr4:9913200-9918000	Weak transcription	Right Atrium	heart
18	chr4:9914000-9917800	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr4:9914200-9926000	Weak transcription	Spleen	Spleen
20	chr4:9914400-9919400	Weak transcription	Duodenum Mucosa	Duodenum
21	chr4:9914400-9922800	Strong transcription	HMEC	breast
22	chr4:9915400-9928000	Strong transcription	Fetal Intestine Small	intestine
23	chr4:9915800-9917400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr4:9916000-9919600	Weak transcription	Fetal Intestine Large	intestine
25	chr4:9916000-9921200	Strong transcription	Liver	Liver
26	chr4:9916600-9916800	Weak transcription	NHEK	skin
27	chr4:9916600-9917400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr4:9916800-9918200	Strong transcription	NHEK	skin
29	chr4:9917000-9922600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr4:9917400-9919600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr4:9917400-9923400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr4:9917600-9918600	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr4:9917800-9918600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr4:9917800-9918600	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr4:9917800-9918800	Enhancers	Lung	lung
36	chr4:9917800-9918800	Enhancers	HSMMtube	muscle
37	chr4:9918000-9918800	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr4:9918000-9920400	Enhancers	Right Atrium	heart
39	chr4:9918200-9919200	Weak transcription	NHEK	skin
40	chr4:9918400-9918600	Active TSS	Pancreas	Pancrea
41	chr4:9918400-9918800	Enhancers	Fetal Muscle Leg	muscle
42	chr4:9918400-9918800	Enhancers	Left Ventricle	heart
43	chr4:9918400-9918800	Enhancers	Psoas Muscle	Psoas
44	chr4:9918400-9919800	Enhancers	Fetal Muscle Trunk	muscle
45	chr4:9918600-9918800	Enhancers	Right Ventricle	heart
46	chr4:9918600-9918800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
47	chr4:9918600-9948600	Weak transcription	Pancreas	Pancrea
48	chr4:9918800-9919400	Weak transcription	Right Ventricle	heart
49	chr4:9918800-9919800	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr4:9918800-9920000	Weak transcription	Lung	lung

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