Variant report

Variant	esv1798614
Chromosome Location	chr11:66514847-66535177
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:88)
CpG islands
(count:366)
Chromatin interactive
region (count:30)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:88 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:66516385-66516459	K562	blood:	n/a	n/a
2	CEBPB	chr11:66532256-66532548	K562	blood:	n/a	chr11:66532389-66532400
3	CEBPB	chr11:66534231-66534466	Hela-S3	cervix:	n/a	chr11:66534358-66534369 chr11:66534360-66534369
4	CEBPB	chr11:66534236-66534492	A549	lung:	n/a	chr11:66534358-66534369 chr11:66534360-66534369
5	CEBPB	chr11:66532163-66532531	MCF-7	breast:	n/a	chr11:66532389-66532400
6	CEBPB	chr11:66532206-66532565	K562	blood:	n/a	chr11:66532389-66532400
7	CEBPB	chr11:66515969-66516115	K562	blood:	n/a	n/a
8	CEBPB	chr11:66532303-66532514	A549	lung:	n/a	chr11:66532389-66532400
9	CEBPB	chr11:66516542-66517221	MCF-7	breast:	n/a	n/a
10	CEBPB	chr11:66534224-66534445	HepG2	liver:	n/a	chr11:66534358-66534369 chr11:66534360-66534369
11	CEBPB	chr11:66532324-66532474	Hela-S3	cervix:	n/a	chr11:66532389-66532400
12	CEBPB	chr11:66532232-66532534	HepG2	liver:	n/a	chr11:66532389-66532400
13	CEBPB	chr11:66532202-66532584	MCF-7	breast:	n/a	chr11:66532389-66532400
14	CEBPB	chr11:66532207-66532662	A549	lung:	n/a	chr11:66532389-66532400
15	CEBPB	chr11:66516086-66516131	Hela-S3	cervix:	n/a	chr11:66516116-66516127
16	CTCF	chr11:66529880-66530030	GM12875	blood:	n/a	n/a
17	CUX1	chr11:66519265-66519313	GM12878	blood:	n/a	n/a
18	EP300	chr11:66516614-66516993	SK-N-SH_RA	brain:	n/a	n/a
19	EP300	chr11:66516463-66516973	T-47D	breast:	n/a	n/a
20	EP300	chr11:66516508-66517017	MCF-7	breast:	n/a	chr11:66516992-66517006
21	EP300	chr11:66516664-66516972	SK-N-SH_RA	brain:	n/a	n/a
22	FOS	chr11:66515991-66516330	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr11:66515330-66515620	MCF10A-Er-Src	breast:	n/a	chr11:66515566-66515578 chr11:66515593-66515602
24	FOS	chr11:66515115-66515631	MCF10A-Er-Src	breast:	n/a	chr11:66515566-66515578 chr11:66515593-66515602
25	FOS	chr11:66515899-66516350	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr11:66515288-66515638	MCF10A-Er-Src	breast:	n/a	chr11:66515566-66515578 chr11:66515593-66515602
27	FOS	chr11:66514972-66516341	HUVEC	blood vessel:	n/a	chr11:66515566-66515578 chr11:66515593-66515602
28	FOS	chr11:66516000-66516300	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr11:66515988-66516321	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr11:66515282-66515696	MCF10A-Er-Src	breast:	n/a	chr11:66515566-66515578 chr11:66515593-66515602
31	FOXA1	chr11:66516476-66516922	T-47D	breast:	n/a	n/a
32	FOXA1	chr11:66516481-66516861	T-47D	breast:	n/a	n/a
33	FOXA1	chr11:66534173-66534458	HepG2	liver:	n/a	n/a
34	GATA3	chr11:66516425-66516849	T-47D	breast:	n/a	n/a
35	GATA3	chr11:66516420-66516848	T-47D	breast:	n/a	n/a
36	GATA3	chr11:66526224-66526506	SH-SY5Y	brain:	n/a	chr11:66526299-66526320
37	GATA3	chr11:66516324-66517054	MCF-7	breast:	n/a	n/a
38	GATA3	chr11:66519479-66519811	SH-SY5Y	brain:	n/a	n/a
39	HDAC2	chr11:66516439-66517016	MCF-7	breast:	n/a	n/a
40	HMGN3	chr11:66529753-66529776	K562	blood:	n/a	n/a
41	JUN	chr11:66531387-66531537	K562	blood:	n/a	n/a
42	JUN	chr11:66534752-66534894	H1-hESC	embryonic stem cell:	n/a	n/a
43	KAP1	chr11:66515048-66515627	U2OS	brain:	n/a	n/a
44	KAP1	chr11:66526520-66526998	K562	blood:	n/a	n/a
45	MAFF	chr11:66519688-66519928	HepG2	liver:	n/a	chr11:66519799-66519817
46	MAFF	chr11:66519693-66519957	K562	blood:	n/a	chr11:66519799-66519817
47	MAFK	chr11:66519718-66519893	Hela-S3	cervix:	n/a	chr11:66519801-66519816
48	MAFK	chr11:66519667-66519924	IMR90	lung:	n/a	chr11:66519801-66519816
49	MAFK	chr11:66519731-66519929	H1-hESC	embryonic stem cell:	n/a	chr11:66519801-66519816
50	MAFK	chr11:66519637-66519948	HepG2	liver:	n/a	chr11:66519801-66519816

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:66529885-66529935	AG04449	skin:	fetal
2	chr11:66529822-66529872	HCT-116	colon:	n/a
3	chr11:66532827-66532877	HCF	heart:	n/a
4	chr11:66529885-66529935	PrEC	prostate:	n/a
5	chr11:66529885-66529935	HRCEpiC	kidney:	n/a
6	chr11:66515382-66515432	Caco-2	colon:	n/a
7	chr11:66529657-66529707	AG10803	skin:	n/a
8	chr11:66515382-66515432	ECC-1	luminal epithelium:	n/a
9	chr11:66530027-66530077	AG04450	lung:	fetal
10	chr11:66529657-66529707	Caco-2	colon:	n/a
11	chr11:66532827-66532877	HAEpiC	amniotic membrane:	n/a
12	chr11:66529822-66529872	HAEpiC	amniotic membrane:	n/a
13	chr11:66530027-66530077	AG04449	skin:	fetal
14	chr11:66529885-66529935	HCPEpiC	choroid plexus:	n/a
15	chr11:66515382-66515432	HEEpiC	esophagus:	n/a
16	chr11:66529822-66529872	IMR90	lung:	fetal
17	chr11:66529657-66529707	HCM	heart:	n/a
18	chr11:66529885-66529935	HRE	kidney:	n/a
19	chr11:66529822-66529872	HRE	kidney:	n/a
20	chr11:66529657-66529707	NT2-D1	testis:	n/a
21	chr11:66532827-66532877	SAEC	small airway:	n/a
22	chr11:66529822-66529872	SAEC	small airway:	n/a
23	chr11:66529885-66529935	NH-A	brain:	n/a
24	chr11:66532827-66532877	HepG2	liver:	n/a
25	chr11:66529822-66529872	K562	blood:	n/a
26	chr11:66529822-66529872	NB4	blood:	n/a
27	chr11:66532827-66532877	U87	brain:	n/a
28	chr11:66532827-66532877	PFSK-1	brain:	n/a
29	chr11:66529885-66529935	PFSK-1	brain:	n/a
30	chr11:66532827-66532877	Hepatocyte	liver:	n/a
31	chr11:66530027-66530077	HCM	heart:	n/a
32	chr11:66532827-66532877	ProgFib	skin:	n/a
33	chr11:66529657-66529707	PrEC	prostate:	n/a
34	chr11:66530027-66530077	Hela-S3	cervix:	n/a
35	chr11:66530027-66530077	K562	blood:	n/a
36	chr11:66515382-66515432	MCF10A-Er-Src	breast:	n/a
37	chr11:66515382-66515432	GM19239	blood:	n/a
38	chr11:66529657-66529707	SAEC	small airway:	n/a
39	chr11:66529657-66529707	AG09319	gingival:	n/a
40	chr11:66529885-66529935	Hepatocyte	liver:	n/a
41	chr11:66529885-66529935	T-47D	breast:	n/a
42	chr11:66530027-66530077	NT2-D1	testis:	n/a
43	chr11:66529885-66529935	HNPCEpiC	eye:	n/a
44	chr11:66530027-66530077	HUVEC	blood vessel:	n/a
45	chr11:66530027-66530077	GM19239	blood:	n/a
46	chr11:66532827-66532877	SK-N-SH_RA	brain:	n/a
47	chr11:66515382-66515432	IMR90	lung:	fetal
48	chr11:66529885-66529935	NHBE	bronchial:	n/a
49	chr11:66529885-66529935	PANC-1	pancreas:	n/a
50	chr11:66515382-66515432	HUVEC	blood vessel:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:66531006..66534192-chr11:66534200..66538203,4	K562	blood:
2	chr11:66516321..66518946-chr11:66520538..66522325,2	K562	blood:
3	chr11:66492885..66503049-chr11:66507993..66515918,26	MCF-7	breast:
4	chr11:66526435..66528204-chr11:66529926..66531450,2	MCF-7	breast:
5	chr11:66495562..66497940-chr11:66534176..66536723,2	K562	blood:
6	chr11:66477252..66477887-chr11:66516349..66517041,2	MCF-7	breast:
7	chr11:66511244..66515622-chr11:66520055..66525870,6	MCF-7	breast:
8	chr11:66531934..66534799-chr11:66536564..66539469,2	MCF-7	breast:
9	chr11:66516509..66519400-chr11:66611915..66614317,2	MCF-7	breast:
10	chr11:66382524..66385340-chr11:66511920..66516933,5	MCF-7	breast:
11	chr11:66510952..66514202-chr11:66524904..66528064,3	K562	blood:
12	chr11:66514864..66517821-chr11:66520272..66522038,2	K562	blood:
13	chr11:66528906..66530759-chr11:66532545..66534201,2	MCF-7	breast:
14	chr11:66493070..66499440-chr11:66510036..66515058,11	K562	blood:
15	chr11:66382727..66385338-chr11:66531188..66533920,2	MCF-7	breast:
16	chr11:66462412..66464688-chr11:66512758..66515188,2	MCF-7	breast:
17	chr11:66493861..66498185-chr11:66524704..66529486,4	K562	blood:
18	chr11:66487345..66489431-chr11:66516687..66519374,2	MCF-7	breast:
19	chr11:66477252..66478002-chr11:66516349..66517231,4	MCF-7	breast:
20	chr11:66443889..66446824-chr11:66516864..66518382,2	MCF-7	breast:
21	chr11:66531006..66534192-chr11:66534200..66538203,4	K562	blood:
22	chr11:66510242..66514990-chr11:66554599..66560135,5	MCF-7	breast:
23	chr11:66492557..66494954-chr11:66515983..66517531,2	K562	blood:
24	chr11:66462840..66465685-chr11:66516258..66519053,2	K562	blood:
25	chr11:66510399..66513984-chr11:66514064..66517719,8	MCF-7	breast:
26	chr11:66512669..66515262-chr17:57923171..57924855,2	MCF-7	breast:
27	chr11:66516321..66518946-chr11:66520538..66522325,2	K562	blood:
28	chr11:66531067..66535329-chr11:66536471..66539126,4	K562	blood:
29	chr11:66508922..66512626-chr11:66532752..66535976,6	MCF-7	breast:
30	chr11:66534456..66536238-chr11:66540459..66542378,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RCE1-1	chr11:66529550-66529921	NONHSAT022351
2	lnc-RCE1-1	chr11:66526514-66526567	NONHSAT022351

No data

Variant related genes	Relation type
ENSG00000213409	TF binding region
C11orf80	TF binding region
ENSG00000213409	CpG island
C11orf80	CpG island
ENSG00000248643	chromatin interactions
ENSG00000254984	chromatin interactions
ENSG00000213409	chromatin interactions
ENSG00000173914	chromatin interactions
ENSG00000173898	chromatin interactions
ENSG00000239306	chromatin interactions
ENSG00000199325	chromatin interactions
ENSG00000173715	chromatin interactions

Extended variants
information (count: 669 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:669 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs512169	chr11:66514847-66514848	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs147573104	chr11:66514859-66514860	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs184508748	chr11:66514898-66514899	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs189387486	chr11:66514916-66514917	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs550491009	chr11:66514940-66514941	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs373886759	chr11:66515092-66515093	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs193127564	chr11:66515096-66515097	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs539237815	chr11:66515109-66515110	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs72925003	chr11:66515115-66515116	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs376985210	chr11:66515118-66515119	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs566191728	chr11:66515149-66515150	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs79814422	chr11:66515182-66515183	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs554741223	chr11:66515239-66515240	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs141969599	chr11:66515318-66515319	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs73505445	chr11:66515335-66515336	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs556841972	chr11:66515349-66515350	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs371093124	chr11:66515361-66515362	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs185573449	chr11:66515373-66515374	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs559094739	chr11:66515380-66515381	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs12272400	chr11:66515382-66515383	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs541943376	chr11:66515389-66515390	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs561618645	chr11:66515486-66515487	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs189124072	chr11:66515511-66515512	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs570443641	chr11:66515541-66515542	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs140543547	chr11:66515596-66515597	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs532819017	chr11:66515602-66515603	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs150463928	chr11:66515736-66515737	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs181460697	chr11:66515749-66515750	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs185707166	chr11:66515821-66515822	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs188854863	chr11:66515823-66515824	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs568418235	chr11:66515968-66515969	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs539234943	chr11:66515974-66515975	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs113830916	chr11:66516007-66516008	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs556904931	chr11:66516040-66516041	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs3782079	chr11:66516049-66516050	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs570549860	chr11:66516071-66516072	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs181246052	chr11:66516099-66516100	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs552832584	chr11:66516126-66516127	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs186073898	chr11:66516195-66516196	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs11227584	chr11:66516230-66516231	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs138326700	chr11:66516259-66516260	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs515829	chr11:66516293-66516294	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs534485526	chr11:66516322-66516323	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs199719581	chr11:66516360-66516361	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs683043	chr11:66516396-66516397	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs77163579	chr11:66516439-66516440	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs190931646	chr11:66516480-66516481	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs575207636	chr11:66516491-66516492	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs183958144	chr11:66516508-66516509	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs544240644	chr11:66516519-66516520	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	19153074	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:66513000-66529000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr11:66513200-66515000	Weak transcription	NH-A	brain
3	chr11:66513200-66515000	Weak transcription	NHDF-Ad	bronchial
4	chr11:66513200-66515200	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr11:66513200-66515200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr11:66513200-66515200	Weak transcription	Lung	lung
7	chr11:66513200-66517600	Weak transcription	Thymus	Thymus
8	chr11:66513200-66521400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr11:66513200-66526600	Weak transcription	Primary hematopoietic stem cells	blood
10	chr11:66513200-66527600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr11:66513200-66530800	Weak transcription	HSMMtube	muscle
12	chr11:66513200-66541200	Weak transcription	Aorta	Aorta
13	chr11:66513200-66555000	Weak transcription	Pancreas	Pancrea
14	chr11:66513400-66515000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:66513400-66515000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr11:66513400-66515000	Weak transcription	K562	blood
17	chr11:66513400-66515800	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr11:66513400-66516400	Weak transcription	NHEK	skin
19	chr11:66513400-66526200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr11:66513400-66527200	Weak transcription	Fetal Thymus	thymus
21	chr11:66513400-66528000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr11:66513400-66528800	Weak transcription	Fetal Muscle Trunk	muscle
23	chr11:66513400-66529600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr11:66513400-66531600	Weak transcription	Rectal Smooth Muscle	rectum
25	chr11:66513400-66540800	Weak transcription	Spleen	Spleen
26	chr11:66513400-66547800	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr11:66513400-66606800	Weak transcription	Brain Angular Gyrus	brain
28	chr11:66513600-66515000	Weak transcription	Esophagus	oesophagus
29	chr11:66513600-66515200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr11:66513600-66515200	Weak transcription	Fetal Brain Male	brain
31	chr11:66513600-66515200	Weak transcription	NHLF	lung
32	chr11:66513600-66526600	Weak transcription	Primary B cells from peripheral blood	blood
33	chr11:66513600-66527000	Weak transcription	Fetal Intestine Small	intestine
34	chr11:66513600-66527600	Weak transcription	Fetal Stomach	stomach
35	chr11:66513600-66528000	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr11:66513600-66529000	Weak transcription	Duodenum Mucosa	Duodenum
37	chr11:66513600-66529000	Weak transcription	Fetal Intestine Large	intestine
38	chr11:66513600-66530400	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr11:66513600-66532600	Weak transcription	Colonic Mucosa	Colon
40	chr11:66513600-66538800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr11:66513800-66515000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr11:66513800-66515000	Weak transcription	Fetal Brain Female	brain
43	chr11:66513800-66515000	Weak transcription	Hela-S3	cervix
44	chr11:66513800-66523200	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr11:66513800-66526000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr11:66513800-66527800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr11:66513800-66528200	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr11:66513800-66529200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr11:66513800-66539800	Weak transcription	GM12878-XiMat	blood
50	chr11:66514000-66515000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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