Variant report

Variant	esv3397718
Chromosome Location	chr22:29278952-29280850
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr22:29279473-29279689	HepG2	liver:	n/a	chr22:29279551-29279560
2	ATF3	chr22:29279478-29279629	K562	blood:	n/a	chr22:29279551-29279560
3	BACH1	chr22:29279533-29279602	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr22:29279963-29280004	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr22:29279396-29280060	K562	blood:	n/a	chr22:29279640-29279656 chr22:29279457-29279473 chr22:29279643-29279659 chr22:29279490-29279506 chr22:29279641-29279657
6	BHLHE40	chr22:29278447-29279161	K562	blood:	n/a	chr22:29278642-29278651 chr22:29278641-29278650 chr22:29278641-29278650
7	BHLHE40	chr22:29279424-29279627	HepG2	liver:	n/a	chr22:29279457-29279473 chr22:29279490-29279506
8	BHLHE40	chr22:29278522-29279769	HepG2	liver:	n/a	chr22:29279640-29279656 chr22:29279457-29279473 chr22:29279643-29279659 chr22:29279490-29279506 chr22:29278642-29278651 chr22:29278641-29278650 chr22:29279641-29279657 chr22:29278641-29278650
9	BHLHE40	chr22:29280016-29280063	GM12878	blood:	n/a	n/a
10	BHLHE40	chr22:29279330-29279751	HepG2	liver:	n/a	chr22:29279640-29279656 chr22:29279457-29279473 chr22:29279643-29279659 chr22:29279490-29279506 chr22:29279641-29279657
11	BHLHE40	chr22:29279400-29279762	GM12878	blood:	n/a	chr22:29279640-29279656 chr22:29279457-29279473 chr22:29279643-29279659 chr22:29279490-29279506 chr22:29279641-29279657
12	BRCA1	chr22:29279494-29279583	Hela-S3	cervix:	n/a	n/a
13	CCNT2	chr22:29278612-29279774	K562	blood:	n/a	chr22:29279418-29279427 chr22:29279408-29279417
14	CEBPB	chr22:29279071-29279430	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr22:29279868-29280076	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr22:29279897-29280088	IMR90	lung:	n/a	n/a
17	CEBPB	chr22:29279946-29280025	K562	blood:	n/a	n/a
18	CEBPD	chr22:29278894-29279304	HepG2	liver:	n/a	n/a
19	CEBPD	chr22:29279365-29279771	HepG2	liver:	n/a	n/a
20	CHD1	chr22:29279972-29280045	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr22:29280737-29280925	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr22:29279898-29280058	K562	blood:	n/a	n/a
23	CHD2	chr22:29279599-29279636	K562	blood:	n/a	chr22:29279606-29279616
24	CHD2	chr22:29279476-29279634	H1-hESC	embryonic stem cell:	n/a	chr22:29279606-29279616
25	CHD2	chr22:29280358-29280359	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr22:29279516-29279591	HepG2	liver:	n/a	n/a
27	CHD2	chr22:29279944-29280126	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr22:29278931-29279515	GM12878	blood:	n/a	chr22:29279409-29279419
29	CHD2	chr22:29278821-29279143	HepG2	liver:	n/a	n/a
30	CHD2	chr22:29278933-29279658	Hela-S3	cervix:	n/a	chr22:29279606-29279616 chr22:29279409-29279419
31	CHD2	chr22:29280527-29280553	HepG2	liver:	n/a	n/a
32	CHD2	chr22:29280047-29280061	HepG2	liver:	n/a	n/a
33	CHD2	chr22:29278823-29279261	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr22:29278891-29279098	K562	blood:	n/a	n/a
35	CREB1	chr22:29278650-29279812	HepG2	liver:	n/a	n/a
36	CREB1	chr22:29278932-29279755	A549	lung:	n/a	n/a
37	CREB1	chr22:29279009-29279748	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr22:29280320-29280470	NHEK	skin:	n/a	n/a
39	CTCF	chr22:29280240-29280390	GM12873	blood:	n/a	n/a
40	CTCF	chr22:29279992-29280104	LNCaP	prostate:	n/a	n/a
41	CTCF	chr22:29280300-29280450	GM12873	blood:	n/a	n/a
42	CTCF	chr22:29280320-29280470	GM06990	blood:	n/a	n/a
43	CTCF	chr22:29280309-29280315	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr22:29280360-29280510	GM12873	blood:	n/a	n/a
45	CTCF	chr22:29280240-29280390	MCF-7	breast:	n/a	n/a
46	CTCF	chr22:29279940-29280090	HMEC	breast:	n/a	n/a
47	CTCF	chr22:29279920-29280070	GM12874	blood:	n/a	n/a
48	CTCF	chr22:29280100-29280250	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr22:29280020-29280170	GM12866	blood:	n/a	chr22:29280088-29280106 chr22:29280090-29280111
50	CTCF	chr22:29280285-29280462	NHEK	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29279129-29279179	HNPCEpiC	eye:	n/a
2	chr22:29279129-29279179	HNPCEpiC	eye:	n/a
3	chr22:29279592-29279642	GM12878	blood:	n/a
4	chr22:29279597-29279647	HIPEpiC	eye:	n/a
5	chr22:29279203-29279253	MCF-7	breast:	n/a
6	chr22:29279967-29280017	CMK	blood:	n/a
7	chr22:29280180-29280230	HAEpiC	amniotic membrane:	n/a
8	chr22:29279967-29280017	AG09319	gingival:	n/a
9	chr22:29279967-29280017	NB4	blood:	n/a
10	chr22:29280180-29280230	T-47D	breast:	n/a
11	chr22:29279967-29280017	Hela-S3	cervix:	n/a
12	chr22:29279597-29279647	SK-N-SH_RA	brain:	n/a
13	chr22:29279592-29279642	NT2-D1	testis:	n/a
14	chr22:29279967-29280017	GM12891	blood:	n/a
15	chr22:29279129-29279179	HEEpiC	esophagus:	n/a
16	chr22:29279203-29279253	AG04449	skin:	fetal
17	chr22:29279203-29279253	HMEC	breast:	n/a
18	chr22:29280180-29280230	HRPEpiC	eye:	n/a
19	chr22:29279967-29280017	BE2_C	brain:	n/a
20	chr22:29279203-29279253	NHBE	bronchial:	n/a
21	chr22:29280180-29280230	HCF	heart:	n/a
22	chr22:29279129-29279179	LNCaP	prostate:	n/a
23	chr22:29279203-29279253	PrEC	prostate:	n/a
24	chr22:29279129-29279179	GM12891	blood:	n/a
25	chr22:29279597-29279647	Jurkat	blood:	n/a
26	chr22:29279129-29279179	PFSK-1	brain:	n/a
27	chr22:29280180-29280230	NB4	blood:	n/a
28	chr22:29279203-29279253	AG10803	skin:	n/a
29	chr22:29279129-29279179	HPAEpiC	pulmonary alveolar:	n/a
30	chr22:29279967-29280017	U87	brain:	n/a
31	chr22:29279967-29280017	GM06990	blood:	n/a
32	chr22:29279129-29279179	SK-N-SH_RA	brain:	n/a
33	chr22:29279592-29279642	SKMC	muscle:	n/a
34	chr22:29279592-29279642	HMEC	breast:	n/a
35	chr22:29279597-29279647	AoSMC	blood vessel:	n/a
36	chr22:29279597-29279647	K562	blood:	n/a
37	chr22:29279203-29279253	RPTEC	kidney:	n/a
38	chr22:29279592-29279642	LNCaP	prostate:	n/a
39	chr22:29280180-29280230	LNCaP	prostate:	n/a
40	chr22:29279592-29279642	RPTEC	kidney:	n/a
41	chr22:29279967-29280017	BJ	skin:	n/a
42	chr22:29279203-29279253	ovcar-3	ovarian:	n/a
43	chr22:29280180-29280230	AG10803	skin:	n/a
44	chr22:29279203-29279253	K562	blood:	n/a
45	chr22:29280180-29280230	ProgFib	skin:	n/a
46	chr22:29279203-29279253	BJ	skin:	n/a
47	chr22:29279592-29279642	MCF-7	breast:	n/a
48	chr22:29279597-29279647	RPTEC	kidney:	n/a
49	chr22:29280180-29280230	HCT-116	colon:	n/a
50	chr22:29279129-29279179	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr22:29277854..29280834-chr3:15899899..15902425,2	MCF-7	breast:
2	chr22:29275977..29281461-chr22:29425203..29430435,9	MCF-7	breast:
3	chr22:29137399..29139735-chr22:29278518..29281229,2	MCF-7	breast:
4	chr22:29280249..29282213-chr22:29433685..29436671,2	MCF-7	breast:
5	chr22:29280662..29283145-chr22:29436035..29437760,2	K562	blood:
6	chr16:31128850..31129465-chr22:29279200..29279987,2	Hela-S3	cervix:
7	chr22:29194507..29196726-chr22:29278986..29282462,3	MCF-7	breast:
8	chr22:29210544..29212146-chr22:29276530..29279392,2	MCF-7	breast:
9	chr22:29274825..29277296-chr22:29277384..29279241,2	K562	blood:
10	chr22:29280624..29284164-chr22:29307760..29311501,3	MCF-7	breast:
11	chr22:29279568..29281765-chr22:29467462..29470387,2	K562	blood:

Variant related genes	Relation type
ZNRF3	TF binding region
ZNRF3	CpG island
ENSG00000272858	chromatin interactions
ENSG00000103510	chromatin interactions
ENSG00000177993	chromatin interactions
ENSG00000183765	chromatin interactions
ENSG00000226471	chromatin interactions
ENSG00000262766	chromatin interactions
ENSG00000206560	chromatin interactions
ENSG00000100209	chromatin interactions
ENSG00000183762	chromatin interactions
ENSG00000100219	chromatin interactions

Extended variants
information (count: 42 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:42 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562057111	chr22:29278953-29278954	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs376173016	chr22:29278979-29278980	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs529316888	chr22:29279011-29279012	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs550752865	chr22:29279021-29279022	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs182230615	chr22:29279023-29279024	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs367558108	chr22:29279107-29279108	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs187549142	chr22:29279129-29279130	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs111464588	chr22:29279132-29279133	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs192486813	chr22:29279136-29279137	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs551529858	chr22:29279152-29279153	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs566829786	chr22:29279162-29279163	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs533824550	chr22:29279206-29279207	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
13	rs555251592	chr22:29279229-29279230	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs374484421	chr22:29279236-29279237	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs116538536	chr22:29279259-29279260	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs184070958	chr22:29279312-29279313	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs575841364	chr22:29279345-29279346	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs374947857	chr22:29279346-29279347	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs555949792	chr22:29279371-29279372	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs115483596	chr22:29279386-29279387	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs544805591	chr22:29279400-29279401	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs547113018	chr22:29279405-29279406	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs573521668	chr22:29279478-29279479	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs375964409	chr22:29279483-29279484	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs540890107	chr22:29279490-29279491	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs188607241	chr22:29279493-29279494	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs529279217	chr22:29279518-29279519	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs544576820	chr22:29279576-29279577	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs562767015	chr22:29279625-29279626	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs1065497	chr22:29279991-29279992	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs73388870	chr22:29280395-29280396	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs118188472	chr22:29280436-29280437	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs527486262	chr22:29280443-29280444	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs200658485	chr22:29280462-29280463	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs74905063	chr22:29280478-29280479	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs78705611	chr22:29280524-29280525	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs537785802	chr22:29280597-29280598	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs556103807	chr22:29280610-29280611	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs571202766	chr22:29280715-29280716	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs538718464	chr22:29280742-29280743	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs553917663	chr22:29280765-29280766	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs201449682	chr22:29280781-29280782	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
abnormal development	18461090	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Cat eye syndrome	16708226	CNVD
Olfactory neuroblastoma	18408657	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29278200-29279000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
2	chr22:29278400-29279000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
3	chr22:29278400-29279000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
4	chr22:29278400-29279000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr22:29278400-29279000	Flanking Active TSS	Fetal Lung	lung
6	chr22:29278400-29279000	Flanking Active TSS	Stomach Smooth Muscle	stomach
7	chr22:29278400-29279000	Flanking Active TSS	HepG2	liver
8	chr22:29278400-29279200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
9	chr22:29278400-29279200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr22:29278400-29279200	Flanking Active TSS	Adipose Nuclei	Adipose
11	chr22:29278400-29279200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr22:29278400-29280400	Active TSS	Brain Cingulate Gyrus	brain
13	chr22:29278600-29279000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
14	chr22:29278600-29279000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr22:29278600-29279000	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr22:29278600-29279000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr22:29278600-29279000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr22:29278600-29279000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
19	chr22:29278600-29279000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
20	chr22:29278600-29279000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
21	chr22:29278600-29279000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
22	chr22:29278600-29279000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr22:29278600-29279000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
24	chr22:29278600-29279000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr22:29278600-29279000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr22:29278600-29279000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr22:29278600-29279000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr22:29278600-29279000	Flanking Active TSS	Liver	Liver
29	chr22:29278600-29279000	Flanking Active TSS	Brain Angular Gyrus	brain
30	chr22:29278600-29279000	Flanking Active TSS	Brain Hippocampus Middle	brain
31	chr22:29278600-29279000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
32	chr22:29278600-29279000	Flanking Active TSS	Duodenum Mucosa	Duodenum
33	chr22:29278600-29279000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
34	chr22:29278600-29279000	Enhancers	Fetal Heart	heart
35	chr22:29278600-29279000	Flanking Active TSS	Fetal Intestine Large	intestine
36	chr22:29278600-29279000	Flanking Active TSS	Fetal Intestine Small	intestine
37	chr22:29278600-29279000	Flanking Active TSS	Placenta	Placenta
38	chr22:29278600-29279000	Flanking Active TSS	Fetal Stomach	stomach
39	chr22:29278600-29279000	Flanking Active TSS	Left Ventricle	heart
40	chr22:29278600-29279000	Flanking Active TSS	Pancreas	Pancrea
41	chr22:29278600-29279000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
42	chr22:29278600-29279000	Flanking Active TSS	Right Ventricle	heart
43	chr22:29278600-29279000	Flanking Active TSS	HUVEC	blood vessel
44	chr22:29278600-29279000	Flanking Active TSS	K562	blood
45	chr22:29278600-29279000	Flanking Active TSS	NHDF-Ad	bronchial
46	chr22:29278600-29279000	Flanking Active TSS	NHEK	skin
47	chr22:29278600-29279000	Flanking Active TSS	Osteobl	bone
48	chr22:29278600-29279200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
49	chr22:29278600-29279200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr22:29278600-29279200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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