Variant report

Variant	nsv962788
Chromosome Location	chr22:32528613-32537754
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	ATF1	chr22:32531984-32532272	K562	blood:	n/a	n/a
2	ATF3	chr22:32532022-32532240	K562	blood:	n/a	n/a
3	BATF	chr22:32533889-32534329	GM12878	blood:	n/a	n/a
4	BHLHE40	chr22:32534000-32534278	GM12878	blood:	n/a	n/a
5	BHLHE40	chr22:32533950-32534208	K562	blood:	n/a	n/a
6	CBX3	chr22:32531989-32532330	HCT-116	colon:	n/a	n/a
7	CEBPB	chr22:32532032-32532344	HCT-116	colon:	n/a	n/a
8	CEBPB	chr22:32533556-32533575	Hela-S3	cervix:	n/a	n/a
9	CTCF	chr22:32536747-32537047	Fibrobl	skin:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
10	CTCF	chr22:32536666-32536951	H1-hESC	embryonic stem cell:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
11	CTCF	chr22:32536680-32536830	GM06990	blood:	n/a	n/a
12	CTCF	chr22:32536756-32536762	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr22:32536680-32536830	AoAF	blood vessel:	n/a	n/a
14	CTCF	chr22:32536820-32536970	GM12873	blood:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
15	CTCF	chr22:32536680-32536830	BE2_C	brain:	n/a	n/a
16	CTCF	chr22:32536735-32537050	MCF-7	breast:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
17	CTCF	chr22:32536800-32536950	AG10803	skin:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
18	CTCF	chr22:32536840-32536990	HCM	heart:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
19	CTCF	chr22:32536745-32537025	MCF-7	breast:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
20	CTCF	chr22:32536733-32537056	GM12892	blood:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
21	CTCF	chr22:32536772-32536850	SK-N-SH_RA	brain:	n/a	n/a
22	CTCF	chr22:32536700-32536850	BE2_C	brain:	n/a	n/a
23	CTCF	chr22:32536787-32537039	LNCaP	prostate:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
24	CTCF	chr22:32536743-32537033	MCF-7	breast:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
25	CTCF	chr22:32536733-32537062	GM12891	blood:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
26	CTCF	chr22:32536820-32536970	GM12872	blood:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
27	CTCF	chr22:32536680-32536830	NB4	blood:	n/a	n/a
28	CTCF	chr22:32537020-32537170	A549	lung:	n/a	n/a
29	CTCF	chr22:32536749-32537036	Gliobla	brain:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
30	CTCF	chr22:32536660-32536810	WI-38	lung:	n/a	n/a
31	CTCF	chr22:32536767-32537033	GM13976	blood:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
32	CTCF	chr22:32536753-32537032	MCF-7	breast:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
33	CTCF	chr22:32532321-32532482	GM10266	blood:	n/a	chr22:32532363-32532381 chr22:32532358-32532379
34	CTCF	chr22:32536752-32537047	GM10248	blood:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
35	CTCF	chr22:32536756-32536995	K562	blood:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
36	CTCF	chr22:32536723-32537066	GM19238	blood:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
37	CTCF	chr22:32536680-32536830	HCT-116	colon:	n/a	n/a
38	CTCF	chr22:32536738-32537052	A549	lung:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
39	CTCF	chr22:32536700-32536850	A549	lung:	n/a	n/a
40	CTCF	chr22:32537669-32537692	GM19239	blood:	n/a	n/a
41	CTCF	chr22:32536680-32536830	MCF-7	breast:	n/a	n/a
42	CTCF	chr22:32536680-32536830	NHEK	skin:	n/a	n/a
43	CTCF	chr22:32536735-32537037	GM19239	blood:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
44	CTCF	chr22:32536640-32536790	HMEC	breast:	n/a	n/a
45	CTCF	chr22:32536723-32536951	HepG2	liver:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
46	CTCF	chr22:32532312-32532426	K562	blood:	n/a	chr22:32532363-32532381 chr22:32532358-32532379
47	CTCF	chr22:32536780-32536930	AG04450	lung:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
48	CTCF	chr22:32532359-32532432	HUVEC	blood vessel:	n/a	chr22:32532363-32532381
49	CTCF	chr22:32536768-32537030	Pancreas_OC	pancreas:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898
50	CTCF	chr22:32536800-32536950	AG09319	gingival:	n/a	chr22:32536881-32536899 chr22:32536884-32536893 chr22:32536884-32536897 chr22:32536886-32536896 chr22:32536883-32536904 chr22:32536884-32536897 chr22:32536882-32536898

No.	Distal block	Cell Line	Cell type	Cell Stage
1	22:32012966-32043914..22:32529813-32538538	K562	blood:
2	22:31836635-31847259..22:32529813-32538538	K562	blood:
3	22:32529813-32538538..22:32764253-32784733	H1-hESC	embryonic stem cell:	embryo
4	22:32529813-32538538..22:32750950-32761732	K562	blood:
5	22:32529813-32538538..22:32860159-32865649	GM12878	blood:
6	22:32529813-32538538..22:32878464-32886640	K562	blood:
7	22:32529813-32538538..22:32868055-32872511	K562	blood:
8	22:32529813-32538538..22:32740683-32750950	H1-hESC	embryonic stem cell:	embryo

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC5A1-1	chr22:32537254-32537326	ENSG00000239674.1

Variant related genes	Relation type
AP1B1P2	TF binding region
ENSG00000239674	TF binding region
ENSG00000271093	chromatin interactions
ENSG00000241954	chromatin interactions
ENSG00000232218	chromatin interactions
ENSG00000241878	chromatin interactions
ENSG00000205853	chromatin interactions
ENSG00000184708	chromatin interactions
ENSG00000100225	chromatin interactions
ENSG00000184459	chromatin interactions
ENSG00000128276	chromatin interactions
ENSG00000230736	chromatin interactions
ENSG00000243519	chromatin interactions

Extended variants
information (count: 381 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:381 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184394703	chr22:32528626-32528627	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs531928797	chr22:32528651-32528652	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368924004	chr22:32528658-32528659	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368059776	chr22:32528667-32528668	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550299030	chr22:32528673-32528674	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563845893	chr22:32528679-32528680	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532814522	chr22:32528713-32528714	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189630734	chr22:32528790-32528791	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145966179	chr22:32528821-32528822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs180845282	chr22:32528826-32528827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535420194	chr22:32528833-32528834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs549239573	chr22:32528854-32528855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138629493	chr22:32528873-32528874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568278894	chr22:32528894-32528895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376779563	chr22:32528903-32528904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79052011	chr22:32528923-32528924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536866745	chr22:32528936-32528937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs370424266	chr22:32528997-32528998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs71313109	chr22:32529041-32529042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs59813439	chr22:32529043-32529044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs398036905	chr22:32529066-32529067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs5753871	chr22:32529089-32529090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs578159335	chr22:32529114-32529115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs35151310	chr22:32529130-32529131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149328263	chr22:32529191-32529192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs553911335	chr22:32529192-32529193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573955530	chr22:32529225-32529226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542996290	chr22:32529242-32529243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs144225497	chr22:32529267-32529268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs576286684	chr22:32529297-32529298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs185026006	chr22:32529312-32529313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs114842657	chr22:32529362-32529363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532881630	chr22:32529416-32529417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546661688	chr22:32529431-32529432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559923413	chr22:32529435-32529436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs115313225	chr22:32529438-32529439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189408482	chr22:32529481-32529482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541318420	chr22:32529514-32529515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181655401	chr22:32529563-32529564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185904371	chr22:32529612-32529613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191218251	chr22:32529613-32529614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs148729522	chr22:32529638-32529639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534314963	chr22:32529679-32529680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573164795	chr22:32529687-32529688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs142031105	chr22:32529689-32529690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7289301	chr22:32529696-32529697	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs112803425	chr22:32529746-32529747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139621436	chr22:32529748-32529749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181566523	chr22:32529808-32529809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144370848	chr22:32529814-32529815	Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
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
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
Endometrioid adenocarcinoma	16974079	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19384346	CNVD
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD
Pancreatic cancer	17952125	CNVD
Autism	19492091	CNVD
Breast cancer	22522925	CNVD
Deafness	17160897	CNVD
Bipolar disorder	19114987	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:231 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:32515800-32533600	Weak transcription	Right Atrium	heart
2	chr22:32528000-32528800	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr22:32528600-32529400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr22:32528600-32529600	Enhancers	Primary T cells fromperipheralblood	blood
5	chr22:32528600-32529600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
6	chr22:32528800-32529200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr22:32528800-32530400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr22:32529000-32529200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr22:32529000-32529600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr22:32529200-32533000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr22:32529200-32533600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr22:32529400-32533000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr22:32529600-32533000	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr22:32529600-32533000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr22:32529600-32533600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr22:32531400-32532200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr22:32531400-32532400	Enhancers	Rectal Mucosa Donor 29	rectum
18	chr22:32531400-32532400	Enhancers	Osteobl	bone
19	chr22:32531400-32532800	Enhancers	HMEC	breast
20	chr22:32531600-32532600	Enhancers	NH-A	brain
21	chr22:32531800-32532400	Enhancers	Muscle Satellite Cultured Cells	--
22	chr22:32531800-32532400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr22:32531800-32532600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr22:32531800-32532600	Enhancers	NHEK	skin
25	chr22:32531800-32532800	Enhancers	HUVEC	blood vessel
26	chr22:32531800-32533000	Enhancers	Left Ventricle	heart
27	chr22:32532000-32532200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr22:32532000-32532200	Enhancers	Spleen	Spleen
29	chr22:32532000-32532400	Enhancers	Dnd41	blood
30	chr22:32532000-32532600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr22:32532200-32532600	Enhancers	Stomach Mucosa	stomach
32	chr22:32532200-32533000	Weak transcription	Spleen	Spleen
33	chr22:32532200-32534000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr22:32532400-32532800	Weak transcription	Dnd41	blood
35	chr22:32532400-32533600	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr22:32532400-32533600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr22:32532400-32533600	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr22:32532600-32533000	Enhancers	K562	blood
39	chr22:32532600-32533600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr22:32532600-32533600	Weak transcription	NHEK	skin
41	chr22:32532600-32533800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr22:32532600-32533800	Weak transcription	Stomach Mucosa	stomach
43	chr22:32532800-32533000	Enhancers	Dnd41	blood
44	chr22:32533000-32533200	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr22:32533000-32533400	Enhancers	Primary T cells fromperipheralblood	blood
46	chr22:32533000-32533400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr22:32533000-32533400	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr22:32533000-32533400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr22:32533000-32533400	Weak transcription	K562	blood
50	chr22:32533000-32533600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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