Variant report

Variant	nsv464069
Chromosome Location	chr6:142322456-142407741
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:826)
CpG islands
(count:244)
Chromatin interactive
region (count:84)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:826 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:142330815-142331218	K562	blood:	n/a	n/a
2	ATF1	chr6:142332981-142333295	K562	blood:	n/a	n/a
3	ATF1	chr6:142351469-142351711	K562	blood:	n/a	n/a
4	ATF1	chr6:142330819-142331132	K562	blood:	n/a	n/a
5	ATF2	chr6:142334418-142334768	GM12878	blood:	n/a	n/a
6	ATF2	chr6:142334470-142334759	GM12878	blood:	n/a	n/a
7	ATF3	chr6:142334431-142334965	HCT-116	colon:	n/a	n/a
8	ATF3	chr6:142332913-142333217	K562	blood:	n/a	n/a
9	BATF	chr6:142334510-142334762	GM12878	blood:	n/a	chr6:142334682-142334692
10	BATF	chr6:142334507-142334749	GM12878	blood:	n/a	chr6:142334682-142334692
11	BATF	chr6:142376411-142376651	GM12878	blood:	n/a	n/a
12	BCL11A	chr6:142336110-142336403	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr6:142334491-142334766	GM12878	blood:	n/a	chr6:142334680-142334689
14	BCL3	chr6:142334415-142334778	GM12878	blood:	n/a	chr6:142334680-142334689
15	BHLHE40	chr6:142343404-142343413	K562	blood:	n/a	n/a
16	BHLHE40	chr6:142366123-142366493	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:142331333-142331472	K562	blood:	n/a	n/a
18	BHLHE40	chr6:142366125-142366500	HepG2	liver:	n/a	n/a
19	BRCA1	chr6:142366297-142366496	GM12878	blood:	n/a	n/a
20	BRCA1	chr6:142327558-142327685	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr6:142348099-142349426	K562	blood:	n/a	n/a
22	CBX3	chr6:142329821-142331711	HCT-116	colon:	n/a	n/a
23	CBX3	chr6:142351172-142351838	K562	blood:	n/a	n/a
24	CBX3	chr6:142348947-142349315	K562	blood:	n/a	n/a
25	CBX3	chr6:142359967-142360532	HCT-116	colon:	n/a	n/a
26	CBX3	chr6:142334322-142334936	HCT-116	colon:	n/a	n/a
27	CBX3	chr6:142348247-142348764	K562	blood:	n/a	n/a
28	CCNT2	chr6:142326311-142326389	K562	blood:	n/a	n/a
29	CEBPB	chr6:142334308-142335016	HCT-116	colon:	n/a	n/a
30	CEBPB	chr6:142334407-142334810	HCT-116	colon:	n/a	n/a
31	CEBPB	chr6:142335610-142335943	IMR90	lung:	n/a	n/a
32	CEBPB	chr6:142349786-142349931	A549	lung:	n/a	n/a
33	CEBPB	chr6:142349796-142349858	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr6:142393174-142393489	HepG2	liver:	n/a	n/a
35	CEBPB	chr6:142366301-142366888	Hela-S3	cervix:	n/a	chr6:142366690-142366701 chr6:142366685-142366702 chr6:142366688-142366701 chr6:142366688-142366699 chr6:142366690-142366701
36	CEBPB	chr6:142366453-142367022	HCT-116	colon:	n/a	chr6:142366690-142366701 chr6:142366685-142366702 chr6:142366688-142366701 chr6:142366688-142366699 chr6:142366690-142366701
37	CEBPB	chr6:142353321-142353541	K562	blood:	n/a	n/a
38	CEBPB	chr6:142334400-142334814	A549	lung:	n/a	n/a
39	CEBPB	chr6:142347600-142348026	MCF-7	breast:	n/a	n/a
40	CEBPB	chr6:142349652-142350283	K562	blood:	n/a	n/a
41	CEBPB	chr6:142407515-142407780	IMR90	lung:	n/a	chr6:142407652-142407663 chr6:142407650-142407663 chr6:142407650-142407663 chr6:142407650-142407663 chr6:142407650-142407661 chr6:142407652-142407663
42	CEBPB	chr6:142334436-142334821	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr6:142334426-142334800	IMR90	lung:	n/a	n/a
44	CEBPB	chr6:142393142-142393543	MCF-7	breast:	n/a	n/a
45	CEBPB	chr6:142366529-142366872	IMR90	lung:	n/a	chr6:142366690-142366701 chr6:142366685-142366702 chr6:142366688-142366701 chr6:142366688-142366699 chr6:142366690-142366701
46	CEBPB	chr6:142343390-142343600	K562	blood:	n/a	n/a
47	CEBPB	chr6:142330492-142331676	HCT-116	colon:	n/a	n/a
48	CEBPB	chr6:142407521-142407816	HepG2	liver:	n/a	chr6:142407652-142407663 chr6:142407650-142407663 chr6:142407650-142407663 chr6:142407650-142407663 chr6:142407650-142407661 chr6:142407652-142407663
49	CEBPB	chr6:142334485-142334802	A549	lung:	n/a	n/a
50	CEBPB	chr6:142334454-142334724	A549	lung:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:142360118-142360168	HRE	kidney:	n/a
2	chr6:142335484-142335534	HMEC	breast:	n/a
3	chr6:142360118-142360168	HepG2	liver:	n/a
4	chr6:142352900-142352950	BE2_C	brain:	n/a
5	chr6:142335484-142335534	NB4	blood:	n/a
6	chr6:142352423-142352473	MCF-7	breast:	n/a
7	chr6:142360118-142360168	HPAEpiC	pulmonary alveolar:	n/a
8	chr6:142352423-142352473	Hepatocyte	liver:	n/a
9	chr6:142335484-142335534	GM19239	blood:	n/a
10	chr6:142335484-142335534	PFSK-1	brain:	n/a
11	chr6:142360118-142360168	GM12878	blood:	n/a
12	chr6:142352900-142352950	GM12891	blood:	n/a
13	chr6:142352423-142352473	A549	lung:	n/a
14	chr6:142335484-142335534	HAEpiC	amniotic membrane:	n/a
15	chr6:142352423-142352473	HEK293	kidney:	embryo
16	chr6:142335484-142335534	HL-60	blood:	n/a
17	chr6:142335484-142335534	CMK	blood:	n/a
18	chr6:142360118-142360168	HAEpiC	amniotic membrane:	n/a
19	chr6:142360118-142360168	HRCEpiC	kidney:	n/a
20	chr6:142352423-142352473	NH-A	brain:	n/a
21	chr6:142360118-142360168	Caco-2	colon:	n/a
22	chr6:142360118-142360168	SK-N-SH	brain:	n/a
23	chr6:142352423-142352473	HUVEC	blood vessel:	n/a
24	chr6:142335484-142335534	HCM	heart:	n/a
25	chr6:142360118-142360168	AG04450	lung:	fetal
26	chr6:142335484-142335534	T-47D	breast:	n/a
27	chr6:142335484-142335534	AG09309	skin:	n/a
28	chr6:142352900-142352950	HRCEpiC	kidney:	n/a
29	chr6:142352423-142352473	ProgFib	skin:	n/a
30	chr6:142335484-142335534	U87	brain:	n/a
31	chr6:142360118-142360168	BJ	skin:	n/a
32	chr6:142352900-142352950	T-47D	breast:	n/a
33	chr6:142352423-142352473	HNPCEpiC	eye:	n/a
34	chr6:142360118-142360168	HMEC	breast:	n/a
35	chr6:142352900-142352950	PrEC	prostate:	n/a
36	chr6:142352423-142352473	HAEpiC	amniotic membrane:	n/a
37	chr6:142352900-142352950	Jurkat	blood:	n/a
38	chr6:142352423-142352473	HEEpiC	esophagus:	n/a
39	chr6:142352423-142352473	AG04450	lung:	fetal
40	chr6:142352900-142352950	NH-A	brain:	n/a
41	chr6:142352423-142352473	NB4	blood:	n/a
42	chr6:142335484-142335534	AG09319	gingival:	n/a
43	chr6:142352423-142352473	SK-N-MC	brain:	n/a
44	chr6:142360118-142360168	HEK293	kidney:	embryo
45	chr6:142360118-142360168	K562	blood:	n/a
46	chr6:142352900-142352950	AG09309	skin:	n/a
47	chr6:142360118-142360168	Hela-S3	cervix:	n/a
48	chr6:142352900-142352950	HUVEC	blood vessel:	n/a
49	chr6:142335484-142335534	HCT-116	colon:	n/a
50	chr6:142335484-142335534	HEEpiC	esophagus:	n/a

(count:84 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:142345393..142347515-chr6:142353520..142355700,2	K562	blood:
2	chr17:41380201..41383708-chr6:142364797..142367825,26	K562	blood:
3	chr17:41398742..41402600-chr6:142364799..142367825,21	K562	blood:
4	chr5:96695823..96698804-chr6:142366314..142367822,2	K562	blood:
5	chr17:41380131..41382207-chr6:142366295..142367824,8	MCF-7	breast:
6	chr6:142379089..142381222-chr6:142382597..142385230,2	K562	blood:
7	chr13:52409628..52411128-chr6:142364817..142366324,2	MCF-7	breast:
8	chr6:142388215..142391078-chr6:142393829..142396159,2	K562	blood:
9	chr11:62607617..62610628-chr6:142364795..142367820,5	K562	blood:
10	chr3:73160527..73161088-chr6:142365825..142366825,2	Hela-S3	cervix:
11	chr6:142388215..142391078-chr6:142393829..142396159,2	K562	blood:
12	chr16:9513156..9513676-chr6:142365801..142366324,2	MCF-7	breast:
13	chr6:142366297..142366801-chrX:77931321..77931822,2	MCF-7	breast:
14	chr6:142342024..142345729-chr6:142348880..142352239,3	K562	blood:
15	chr6:142310160..142310940-chr6:142392407..142393314,2	MCF-7	breast:
16	chr11:62607631..62609197-chr6:142364799..142366321,4	MCF-7	breast:
17	chr19:49943464..49943982-chr6:142365804..142366321,2	Hela-S3	cervix:
18	chr17:41398699..41402637-chr6:142364804..142367821,8	MCF-7	breast:
19	chr6:141962578..141963250-chr6:142366256..142367149,2	MCF-7	breast:
20	chr3:73159944..73162090-chr6:142364797..142366302,3	MCF-7	breast:
21	chr6:142382809..142385096-chr6:142386866..142388393,2	K562	blood:
22	chr17:41391510..41393303-chr6:142364805..142367822,3	K562	blood:
23	chr6:106716720..106717223-chr6:142365820..142366802,2	Hela-S3	cervix:
24	chr10:103124607..103126130-chr6:142364797..142366317,3	K562	blood:
25	chr6:142331145..142333500-chr6:142346672..142348652,2	K562	blood:
26	chr22:50800361..50801881-chr6:142366303..142367821,2	K562	blood:
27	chr6:142366297..142366805-chr8:21899435..21899935,2	Hela-S3	cervix:
28	chr3:73160094..73162090-chr6:142364795..142366316,3	MCF-7	breast:
29	chr17:41399314..41402537-chr6:142366296..142367823,5	MCF-7	breast:
30	chr6:142366315..142366817-chr9:100684493..100685268,2	Hela-S3	cervix:
31	chr6:142365797..142366794-chr8:23398448..23399114,2	Hela-S3	cervix:
32	chr12:46766043..46766884-chr6:142365797..142366324,2	Hela-S3	cervix:
33	chr6:142309853..142311057-chr6:142366249..142367364,12	MCF-7	breast:
34	chr6:142365543..142367464-chr6:142370102..142372383,2	K562	blood:
35	chr5:133457468..133458988-chr6:142366303..142367825,3	K562	blood:
36	chr3:73159958..73160528-chr6:142365797..142366324,3	HCT-116	colon:
37	chr3:73160568..73161090-chr6:142365795..142366302,2	HCT-116	colon:
38	chr11:69463942..69465442-chr6:142366315..142367823,2	K562	blood:
39	chr17:41462176..41466216-chr6:142364797..142367825,8	MCF-7	breast:
40	chr6:142342024..142345729-chr6:142348880..142352239,3	K562	blood:
41	chr21:43172983..43173483-chr6:142366294..142366805,2	Hela-S3	cervix:
42	chr2:18029840..18030360-chr6:142365802..142366315,2	MCF-7	breast:
43	chr17:41391026..41393127-chr6:142366322..142367825,2	K562	blood:
44	chr6:142310115..142310645-chr6:142364498..142365481,2	MCF-7	breast:
45	chr17:41463781..41464354-chr6:142366301..142366821,2	MCF-7	breast:
46	chr6:142366316..142367825-chrX:77930343..77931843,2	K562	blood:
47	chr17:41380090..41383896-chr6:142364797..142367825,21	K562	blood:
48	chr2:106399775..106401275-chr6:142364820..142367803,2	MCF-7	breast:
49	chr6:142345393..142347515-chr6:142353520..142355700,2	K562	blood:
50	chr2:20500446..20501966-chr6:142366297..142367819,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GJE1-6	chr6:142383854-142384190	NONHSAT115302

No data

Variant related genes	Relation type
ENSG00000270983	TF binding region
ENSG00000236822	TF binding region
NMBR	TF binding region
ENSG00000270983	CpG island
ENSG00000236822	CpG island
NMBR	CpG island
ENSG00000223247	chromatin interactions
ENSG00000104888	chromatin interactions
ENSG00000257199	chromatin interactions
ENSG00000104907	chromatin interactions
ENSG00000136932	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000158815	chromatin interactions
ENSG00000147454	chromatin interactions
ENSG00000222414	chromatin interactions
ENSG00000173852	chromatin interactions
ENSG00000270983	chromatin interactions
ENSG00000134294	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 2445 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2445 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9385984	chr6:142322456-142322457	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192216383	chr6:142322529-142322530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542686819	chr6:142322574-142322575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184282221	chr6:142322582-142322583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs187927471	chr6:142322583-142322584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143304731	chr6:142322676-142322677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs193096916	chr6:142322712-142322713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185508826	chr6:142322718-142322719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532749030	chr6:142322727-142322728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547639877	chr6:142322736-142322737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs189217403	chr6:142322765-142322766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530160648	chr6:142322782-142322783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs180756543	chr6:142322783-142322784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs373476101	chr6:142322789-142322790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548683237	chr6:142322798-142322799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147103415	chr6:142322800-142322801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537437527	chr6:142322904-142322905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568987000	chr6:142322925-142322926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs75261532	chr6:142323049-142323050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77920474	chr6:142323160-142323161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538851498	chr6:142323181-142323182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs75668047	chr6:142323201-142323202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528895763	chr6:142323217-142323218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572190490	chr6:142323226-142323227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535983264	chr6:142323227-142323228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73779899	chr6:142323239-142323240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184271452	chr6:142323245-142323246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542972705	chr6:142323251-142323252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs78846046	chr6:142323323-142323324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146907434	chr6:142323346-142323347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577440450	chr6:142323352-142323353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567764404	chr6:142323368-142323369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115954138	chr6:142323399-142323400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553105294	chr6:142323409-142323410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559729187	chr6:142323420-142323421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530302724	chr6:142323442-142323443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs138541457	chr6:142323524-142323525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548745440	chr6:142323534-142323535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs397790942	chr6:142323536-142323537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542529047	chr6:142323564-142323565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113630454	chr6:142323596-142323597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200163758	chr6:142323606-142323607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561996028	chr6:142323607-142323608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373881912	chr6:142323608-142323609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113756018	chr6:142323627-142323628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143804237	chr6:142323638-142323639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552579516	chr6:142323653-142323654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538989931	chr6:142323760-142323761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs114677113	chr6:142323807-142323808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538590839	chr6:142323846-142323847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	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
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
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	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
Breast cancer	21364760	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute monocytic leukemia	16498392	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
craniofacial dysmorphism	21918468	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Burkitt''s lymphoma	19759907	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142310800-142334400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:142311000-142329000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:142312200-142329000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr6:142320800-142330200	Weak transcription	HSMM	muscle
5	chr6:142322200-142324200	Weak transcription	K562	blood
6	chr6:142324200-142324400	Enhancers	K562	blood
7	chr6:142324400-142324600	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr6:142324400-142324600	Active TSS	Muscle Satellite Cultured Cells	--
9	chr6:142324400-142324600	Genic enhancers	K562	blood
10	chr6:142324600-142326200	Weak transcription	K562	blood
11	chr6:142324600-142335000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr6:142326200-142326600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr6:142326200-142326800	Enhancers	K562	blood
14	chr6:142326800-142330000	Weak transcription	K562	blood
15	chr6:142328000-142329200	Weak transcription	HMEC	breast
16	chr6:142329000-142329400	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr6:142329000-142329400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:142329000-142329800	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr6:142329000-142332400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr6:142329000-142333400	Enhancers	Hela-S3	cervix
21	chr6:142329200-142329400	Enhancers	H1 Cell Line	embryonic stem cell
22	chr6:142329200-142329400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr6:142329200-142331200	Enhancers	HMEC	breast
24	chr6:142329200-142331200	Enhancers	NHEK	skin
25	chr6:142329200-142331600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr6:142329400-142330400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr6:142329400-142330600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr6:142329400-142335000	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr6:142329400-142335000	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr6:142329800-142330600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr6:142329800-142334400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr6:142330000-142330400	Enhancers	K562	blood
33	chr6:142330000-142330600	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr6:142330000-142335000	Enhancers	NH-A	brain
35	chr6:142330000-142335400	Enhancers	NHDF-Ad	bronchial
36	chr6:142330200-142333000	Enhancers	HSMMtube	muscle
37	chr6:142330200-142333200	Enhancers	HSMM	muscle
38	chr6:142330200-142335000	Enhancers	NHLF	lung
39	chr6:142330400-142331000	Flanking Active TSS	K562	blood
40	chr6:142330400-142331200	Enhancers	Fetal Heart	heart
41	chr6:142330400-142331400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr6:142330400-142331400	Enhancers	Placenta Amnion	Placenta Amnion
43	chr6:142330400-142331600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr6:142330400-142331600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr6:142330400-142333200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr6:142330400-142335000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr6:142330400-142335000	Enhancers	Muscle Satellite Cultured Cells	--
48	chr6:142330400-142335000	Enhancers	Osteobl	bone
49	chr6:142330600-142331000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr6:142330600-142331200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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