Variant report

Variant	nsv1016007
Chromosome Location	chr6:15099585-15159098
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:542)
CpG islands
(count:183)
Chromatin interactive
region (count:54)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:542 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:15106725-15107548	K562	blood:	n/a	n/a
2	ATF1	chr6:15121792-15121851	K562	blood:	n/a	n/a
3	ATF2	chr6:15137321-15137716	GM12878	blood:	n/a	n/a
4	ATF2	chr6:15151311-15151869	GM12878	blood:	n/a	n/a
5	ATF3	chr6:15144832-15145213	K562	blood:	n/a	n/a
6	ATF3	chr6:15133116-15133632	A549	lung:	n/a	n/a
7	BACH1	chr6:15131621-15131806	K562	blood:	n/a	n/a
8	BACH1	chr6:15122347-15122763	K562	blood:	n/a	n/a
9	BACH1	chr6:15109371-15109372	K562	blood:	n/a	n/a
10	BATF	chr6:15150444-15150764	GM12878	blood:	n/a	chr6:15150606-15150617
11	BATF	chr6:15137335-15137660	GM12878	blood:	n/a	n/a
12	BATF	chr6:15137326-15137576	GM12878	blood:	n/a	n/a
13	BATF	chr6:15151444-15151726	GM12878	blood:	n/a	n/a
14	BCL11A	chr6:15151369-15151810	GM12878	blood:	n/a	n/a
15	BCL3	chr6:15133100-15133556	A549	lung:	n/a	chr6:15133398-15133407
16	BCLAF1	chr6:15151358-15151813	GM12878	blood:	n/a	n/a
17	BCLAF1	chr6:15151355-15151858	GM12878	blood:	n/a	n/a
18	BHLHE40	chr6:15148768-15149053	HepG2	liver:	n/a	n/a
19	BHLHE40	chr6:15106719-15107788	K562	blood:	n/a	n/a
20	BHLHE40	chr6:15148784-15148998	GM12878	blood:	n/a	n/a
21	BHLHE40	chr6:15151478-15151810	GM12878	blood:	n/a	n/a
22	CBX3	chr6:15132935-15133974	HCT-116	colon:	n/a	n/a
23	CBX3	chr6:15122363-15122748	K562	blood:	n/a	n/a
24	CBX3	chr6:15132786-15134075	HCT-116	colon:	n/a	n/a
25	CBX3	chr6:15106008-15107878	K562	blood:	n/a	n/a
26	CCNT2	chr6:15107227-15107846	K562	blood:	n/a	chr6:15107707-15107716
27	CEBPB	chr6:15144837-15145214	Hela-S3	cervix:	n/a	chr6:15145015-15145026
28	CEBPB	chr6:15132823-15134089	HCT-116	colon:	n/a	n/a
29	CEBPB	chr6:15133083-15133685	A549	lung:	n/a	n/a
30	CEBPB	chr6:15144834-15145214	K562	blood:	n/a	chr6:15145015-15145026
31	CEBPB	chr6:15144715-15145302	HCT-116	colon:	n/a	chr6:15145015-15145026
32	CEBPB	chr6:15144885-15145119	K562	blood:	n/a	chr6:15145015-15145026
33	CEBPB	chr6:15133098-15133554	A549	lung:	n/a	n/a
34	CEBPB	chr6:15132932-15133755	A549	lung:	n/a	n/a
35	CEBPB	chr6:15144839-15145157	HepG2	liver:	n/a	chr6:15145015-15145026
36	CEBPB	chr6:15101556-15101609	H1-hESC	embryonic stem cell:	n/a	chr6:15101585-15101596
37	CEBPB	chr6:15139086-15139332	K562	blood:	n/a	chr6:15139172-15139183
38	CEBPB	chr6:15111208-15111557	HepG2	liver:	n/a	chr6:15111375-15111386
39	CEBPB	chr6:15107164-15107551	K562	blood:	n/a	n/a
40	CEBPB	chr6:15134524-15134739	A549	lung:	n/a	n/a
41	CEBPB	chr6:15101551-15101606	HepG2	liver:	n/a	chr6:15101585-15101596
42	CEBPB	chr6:15108823-15109087	H1-hESC	embryonic stem cell:	n/a	chr6:15108962-15108973 chr6:15108963-15108974 chr6:15108962-15108975
43	CEBPB	chr6:15144902-15145200	MCF-7	breast:	n/a	chr6:15145015-15145026
44	CEBPB	chr6:15150602-15150767	HepG2	liver:	n/a	chr6:15150672-15150683 chr6:15150673-15150684 chr6:15150631-15150639 chr6:15150672-15150683 chr6:15150672-15150685 chr6:15150672-15150685
45	CEBPB	chr6:15156262-15156533	K562	blood:	n/a	n/a
46	CEBPB	chr6:15133187-15133555	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr6:15144941-15145213	A549	lung:	n/a	chr6:15145015-15145026
48	CEBPB	chr6:15134634-15134765	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:15144879-15145141	HepG2	liver:	n/a	chr6:15145015-15145026
50	CEBPB	chr6:15145011-15145062	H1-hESC	embryonic stem cell:	n/a	chr6:15145015-15145026

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:15149029-15149079	AG09309	skin:	n/a
2	chr6:15133183-15133233	K562	blood:	n/a
3	chr6:15143233-15143283	SAEC	small airway:	n/a
4	chr6:15143233-15143283	SKMC	muscle:	n/a
5	chr6:15149029-15149079	CMK	blood:	n/a
6	chr6:15149029-15149079	SK-N-MC	brain:	n/a
7	chr6:15133183-15133233	NHDF-neo	bronchial:	n/a
8	chr6:15149029-15149079	ProgFib	skin:	n/a
9	chr6:15133183-15133233	SAEC	small airway:	n/a
10	chr6:15133183-15133233	HNPCEpiC	eye:	n/a
11	chr6:15143233-15143283	HCF	heart:	n/a
12	chr6:15133183-15133233	NT2-D1	testis:	n/a
13	chr6:15143233-15143283	BJ	skin:	n/a
14	chr6:15133183-15133233	Hepatocyte	liver:	n/a
15	chr6:15149029-15149079	NHBE	bronchial:	n/a
16	chr6:15149029-15149079	NH-A	brain:	n/a
17	chr6:15133183-15133233	HAEpiC	amniotic membrane:	n/a
18	chr6:15143233-15143283	GM06990	blood:	n/a
19	chr6:15133183-15133233	NH-A	brain:	n/a
20	chr6:15149029-15149079	SKMC	muscle:	n/a
21	chr6:15143233-15143283	HPAEpiC	pulmonary alveolar:	n/a
22	chr6:15143233-15143283	K562	blood:	n/a
23	chr6:15133183-15133233	ovcar-3	ovarian:	n/a
24	chr6:15133183-15133233	HCF	heart:	n/a
25	chr6:15133183-15133233	HRPEpiC	eye:	n/a
26	chr6:15149029-15149079	Hela-S3	cervix:	n/a
27	chr6:15149029-15149079	NT2-D1	testis:	n/a
28	chr6:15133183-15133233	MCF10A-Er-Src	breast:	n/a
29	chr6:15143233-15143283	AG09309	skin:	n/a
30	chr6:15143233-15143283	AG04449	skin:	fetal
31	chr6:15143233-15143283	ovcar-3	ovarian:	n/a
32	chr6:15149029-15149079	AG04450	lung:	fetal
33	chr6:15143233-15143283	NB4	blood:	n/a
34	chr6:15149029-15149079	HPAEpiC	pulmonary alveolar:	n/a
35	chr6:15149029-15149079	GM06990	blood:	n/a
36	chr6:15143233-15143283	HCM	heart:	n/a
37	chr6:15143233-15143283	Jurkat	blood:	n/a
38	chr6:15149029-15149079	A549	lung:	n/a
39	chr6:15133183-15133233	SKMC	muscle:	n/a
40	chr6:15143233-15143283	HCT-116	colon:	n/a
41	chr6:15143233-15143283	HIPEpiC	eye:	n/a
42	chr6:15143233-15143283	HepG2	liver:	n/a
43	chr6:15149029-15149079	Hepatocyte	liver:	n/a
44	chr6:15149029-15149079	HepG2	liver:	n/a
45	chr6:15149029-15149079	GM12878	blood:	n/a
46	chr6:15149029-15149079	HIPEpiC	eye:	n/a
47	chr6:15149029-15149079	HRCEpiC	kidney:	n/a
48	chr6:15143233-15143283	AG09319	gingival:	n/a
49	chr6:15133183-15133233	HCPEpiC	choroid plexus:	n/a
50	chr6:15149029-15149079	ovcar-3	ovarian:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:15136761..15139272-chr6:15149097..15150701,2	MCF-7	breast:
2	chr6:15144340..15146667-chr6:15148737..15150328,2	K562	blood:
3	chr6:15156210..15158890-chr6:15211476..15214661,3	K562	blood:
4	chr6:15107869..15110295-chr6:15242346..15245809,3	K562	blood:
5	chr6:15102630..15105132-chr6:15106724..15108823,2	K562	blood:
6	chr6:15097373..15100226-chr6:15101243..15103987,3	K562	blood:
7	chr6:15143619..15146318-chr6:15151883..15153386,2	MCF-7	breast:
8	chr6:15088965..15090791-chr6:15157951..15160766,2	K562	blood:
9	chr6:15158330..15160167-chr6:15160268..15162625,2	K562	blood:
10	chr6:14882855..14884940-chr6:15106180..15108933,2	K562	blood:
11	chr6:15119436..15121863-chr6:15121946..15124173,2	K562	blood:
12	chr6:15143619..15146318-chr6:15151883..15153386,2	MCF-7	breast:
13	chr6:15099407..15102397-chr6:15106486..15108344,2	K562	blood:
14	chr6:15133229..15135738-chr6:15147564..15149146,2	K562	blood:
15	chr6:15143787..15146280-chr6:15158034..15160190,2	K562	blood:
16	chr6:15131659..15133367-chr6:15138303..15139913,2	K562	blood:
17	chr6:15120083..15121964-chr6:15210438..15212064,2	K562	blood:
18	chr6:15105604..15108959-chr6:15245974..15248979,5	K562	blood:
19	chr6:15119436..15121863-chr6:15121946..15124173,2	K562	blood:
20	chr6:15103877..15106260-chr6:15135421..15138243,2	K562	blood:
21	chr6:15132794..15134906-chr6:15135026..15137692,3	K562	blood:
22	chr6:15130172..15131963-chr6:15134360..15137201,2	K562	blood:
23	chr6:15143787..15146280-chr6:15158034..15160190,2	K562	blood:
24	chr6:15132794..15134906-chr6:15135026..15137692,3	K562	blood:
25	chr6:15155665..15157322-chr6:15249355..15251263,2	K562	blood:
26	chr6:15092995..15095757-chr6:15118674..15121139,2	K562	blood:
27	chr6:15147856..15151805-chr6:15244004..15248641,4	MCF-7	breast:
28	chr6:15125739..15127625-chr6:15128414..15130165,2	MCF-7	breast:
29	chr6:15097373..15100226-chr6:15101243..15103987,3	K562	blood:
30	chr6:15069954..15071516-chr6:15106946..15109346,2	K562	blood:
31	chr6:14918253..14920493-chr6:15156735..15158710,2	MCF-7	breast:
32	chr6:15110076..15111884-chr6:15115512..15117432,2	K562	blood:
33	chr6:15148839..15151214-chr6:15151716..15153395,2	MCF-7	breast:
34	chr6:15131659..15133367-chr6:15138303..15139913,2	K562	blood:
35	chr6:15086616..15088953-chr6:15137602..15139748,2	K562	blood:
36	chr6:15092731..15095339-chr6:15106274..15108820,2	K562	blood:
37	chr6:15089015..15091067-chr6:15101171..15103884,2	K562	blood:
38	chr6:15106983..15108831-chr6:15151531..15154353,2	K562	blood:
39	chr6:15106242..15108900-chr6:15209959..15212920,4	K562	blood:
40	chr6:15103632..15105300-chr6:15106507..15108224,2	K562	blood:
41	chr6:15136573..15138156-chr6:15245614..15247177,2	K562	blood:
42	chr6:14778863..14781243-chr6:15107030..15109161,2	K562	blood:
43	chr6:15133229..15135738-chr6:15147564..15149146,2	K562	blood:
44	chr6:15130172..15131963-chr6:15134360..15137201,2	K562	blood:
45	chr6:15093162..15095883-chr6:15107253..15109539,2	MCF-7	breast:
46	chr6:15106427..15109667-chr6:15111584..15114479,3	K562	blood:
47	chr6:15134521..15137153-chr6:15210415..15211932,2	K562	blood:
48	chr6:15106983..15108831-chr6:15151531..15154353,2	K562	blood:
49	chr6:15084562..15086829-chr6:15124067..15125929,2	K562	blood:
50	chr6:15096022..15098594-chr6:15145992..15148961,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DTNBP1-12	chr6:15105626-15105685	NONHSAT107863
2	lnc-DTNBP1-11	chr6:15103177-15103313	NONHSAT107864
3	lnc-DTNBP1-11	chr6:15103630-15104361	NONHSAT107864
4	lnc-JARID2-3	chr6:15113199-15113450	NONHSAT107865

No data

Variant related genes	Relation type
ENSG00000216754	TF binding region
RN7SL332P	TF binding region
ENSG00000264687	TF binding region
ENSG00000216754	CpG island
RN7SL332P	CpG island
ENSG00000264687	CpG island
ENSG00000234261	chromatin interactions
ENSG00000271888	chromatin interactions
ENSG00000235488	chromatin interactions
ENSG00000264687	chromatin interactions
ENSG00000008083	chromatin interactions
ENSG00000216754	chromatin interactions
ENSG00000242989	chromatin interactions

Extended variants
information (count: 2306 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2306 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9370792	chr6:15099585-15099586	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs374432310	chr6:15099597-15099598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs367660334	chr6:15099679-15099680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs13191059	chr6:15099687-15099688	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs186337657	chr6:15099695-15099696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114293921	chr6:15099696-15099697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs4715964	chr6:15099716-15099717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs9800553	chr6:15099728-15099729	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs151053759	chr6:15099765-15099766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543945367	chr6:15099773-15099774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563683175	chr6:15099774-15099775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532656024	chr6:15099784-15099785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551788624	chr6:15099791-15099792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558899700	chr6:15099797-15099798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191745528	chr6:15099798-15099799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201809743	chr6:15099824-15099825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547994543	chr6:15099829-15099830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568108554	chr6:15099850-15099851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182875430	chr6:15099854-15099855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550793169	chr6:15099906-15099907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs570802176	chr6:15099926-15099927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569844941	chr6:15100004-15100005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs72832884	chr6:15100024-15100025	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs559021346	chr6:15100029-15100030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572373905	chr6:15100065-15100066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553691206	chr6:15100104-15100105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187865682	chr6:15100118-15100119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554765823	chr6:15100172-15100173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1739084	chr6:15100301-15100302	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs111942420	chr6:15100310-15100311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs9370793	chr6:15100339-15100340	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs113053462	chr6:15100422-15100423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546108852	chr6:15100428-15100429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12198828	chr6:15100481-15100482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35821948	chr6:15100491-15100492	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs541763437	chr6:15100505-15100506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192423759	chr6:15100545-15100546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78621831	chr6:15100568-15100569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145914523	chr6:15100645-15100646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs561375508	chr6:15100693-15100694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs13196118	chr6:15100696-15100697	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs181386587	chr6:15100732-15100733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183104168	chr6:15100750-15100751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111929950	chr6:15100780-15100781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533135475	chr6:15100795-15100796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546934211	chr6:15100798-15100799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566709281	chr6:15100828-15100829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187664104	chr6:15100840-15100841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144346934	chr6:15100841-15100842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192518567	chr6:15100845-15100846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
abnormal development	18461090	CNVD
Cancer	16790693	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21785460	CNVD

Chromatin state (count:277 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15087400-15117600	Weak transcription	Right Atrium	heart
2	chr6:15090400-15109000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:15098400-15103600	Weak transcription	K562	blood
4	chr6:15102400-15103200	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr6:15103600-15104800	Enhancers	K562	blood
6	chr6:15104800-15106600	Weak transcription	K562	blood
7	chr6:15106600-15106800	Enhancers	K562	blood
8	chr6:15106800-15108000	Flanking Active TSS	K562	blood
9	chr6:15107000-15107800	Enhancers	H1 Cell Line	embryonic stem cell
10	chr6:15107400-15108200	Enhancers	Fetal Stomach	stomach
11	chr6:15107400-15109200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr6:15107800-15108800	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr6:15108000-15108400	Enhancers	Fetal Brain Female	brain
14	chr6:15108000-15109200	Enhancers	K562	blood
15	chr6:15108400-15109200	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr6:15108400-15110600	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr6:15108600-15110000	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr6:15108800-15109400	Enhancers	H1 Cell Line	embryonic stem cell
19	chr6:15108800-15109400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr6:15109000-15109400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr6:15109000-15109400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr6:15109000-15109400	Enhancers	Fetal Lung	lung
23	chr6:15109000-15109400	Enhancers	Pancreas	Pancrea
24	chr6:15109000-15109600	Enhancers	Primary B cells from cord blood	blood
25	chr6:15109000-15109600	Enhancers	Fetal Intestine Large	intestine
26	chr6:15109000-15110000	Enhancers	Fetal Brain Male	brain
27	chr6:15109000-15110400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr6:15109200-15109600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr6:15109200-15111000	Weak transcription	K562	blood
30	chr6:15109400-15115800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr6:15109400-15116200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr6:15109600-15109800	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr6:15110600-15114800	Weak transcription	Primary neutrophils fromperipheralblood	blood
34	chr6:15111000-15112000	Enhancers	K562	blood
35	chr6:15111400-15112000	Enhancers	Fetal Thymus	thymus
36	chr6:15112000-15113800	Weak transcription	K562	blood
37	chr6:15113800-15114200	Enhancers	K562	blood
38	chr6:15114800-15116200	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr6:15115800-15116200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr6:15115800-15116200	Weak transcription	Aorta	Aorta
41	chr6:15115800-15116400	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr6:15116200-15116400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr6:15116200-15116400	Enhancers	Aorta	Aorta
44	chr6:15116400-15117200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr6:15116400-15132000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr6:15117000-15117400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr6:15117200-15117600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr6:15121400-15122400	Enhancers	Fetal Thymus	thymus
49	chr6:15121600-15122000	Enhancers	Thymus	Thymus
50	chr6:15121800-15122800	Enhancers	K562	blood

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