Variant report

Variant	nsv960938
Chromosome Location	chr19:21766627-21785276
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:162)
CpG islands
(count:366)
Chromatin interactive
region (count:6)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:162 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:21784781-21786180	K562	blood:	n/a	n/a
2	ARID3A	chr19:21776657-21777194	K562	blood:	n/a	n/a
3	ARID3A	chr19:21775949-21776229	K562	blood:	n/a	n/a
4	ATF1	chr19:21775871-21777447	K562	blood:	n/a	n/a
5	ATF3	chr19:21776694-21777184	K562	blood:	n/a	n/a
6	BACH1	chr19:21783750-21783899	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr19:21769790-21769935	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr19:21777662-21777846	K562	blood:	n/a	n/a
9	BACH1	chr19:21775825-21776466	K562	blood:	n/a	n/a
10	BHLHE40	chr19:21785096-21785106	K562	blood:	n/a	n/a
11	BHLHE40	chr19:21782352-21782391	K562	blood:	n/a	n/a
12	BHLHE40	chr19:21775428-21777483	K562	blood:	n/a	n/a
13	CBX3	chr19:21775702-21776564	K562	blood:	n/a	n/a
14	CBX3	chr19:21776630-21777275	K562	blood:	n/a	n/a
15	CCNT2	chr19:21775821-21776167	K562	blood:	n/a	n/a
16	CCNT2	chr19:21776451-21777013	K562	blood:	n/a	n/a
17	CCNT2	chr19:21769328-21769513	K562	blood:	n/a	n/a
18	CEBPB	chr19:21779625-21780840	HepG2	liver:	n/a	n/a
19	CEBPB	chr19:21776793-21777722	IMR90	lung:	n/a	n/a
20	CEBPB	chr19:21776819-21777845	A549	lung:	n/a	n/a
21	CEBPB	chr19:21775847-21776313	K562	blood:	n/a	n/a
22	CEBPB	chr19:21778851-21779309	A549	lung:	n/a	chr19:21779166-21779177
23	CEBPB	chr19:21778143-21778441	K562	blood:	n/a	n/a
24	CEBPB	chr19:21776674-21777255	K562	blood:	n/a	n/a
25	CEBPB	chr19:21779780-21780285	A549	lung:	n/a	n/a
26	CEBPB	chr19:21776721-21777179	MCF-7	breast:	n/a	n/a
27	CEBPB	chr19:21780602-21780802	K562	blood:	n/a	n/a
28	CEBPB	chr19:21778884-21779346	HepG2	liver:	n/a	chr19:21779166-21779177
29	CEBPB	chr19:21776359-21777781	K562	blood:	n/a	n/a
30	CEBPB	chr19:21778762-21779266	K562	blood:	n/a	chr19:21779166-21779177
31	CEBPB	chr19:21778858-21779344	IMR90	lung:	n/a	chr19:21779166-21779177
32	CEBPB	chr19:21785177-21786277	K562	blood:	n/a	chr19:21785284-21785292
33	CEBPB	chr19:21779688-21780694	IMR90	lung:	n/a	n/a
34	CEBPB	chr19:21776570-21777936	K562	blood:	n/a	n/a
35	CEBPB	chr19:21778754-21780344	K562	blood:	n/a	chr19:21779166-21779177
36	CEBPB	chr19:21776753-21777706	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr19:21778158-21778442	HepG2	liver:	n/a	n/a
38	CEBPB	chr19:21776767-21777855	HepG2	liver:	n/a	n/a
39	CEBPB	chr19:21778178-21778395	IMR90	lung:	n/a	n/a
40	CEBPD	chr19:21776717-21777326	K562	blood:	n/a	n/a
41	CEBPD	chr19:21776575-21777326	K562	blood:	n/a	n/a
42	CHD2	chr19:21769126-21769272	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr19:21769200-21769350	NHEK	skin:	n/a	n/a
44	CTCF	chr19:21783995-21784195	K562	blood:	n/a	n/a
45	CTCF	chr19:21771492-21771553	Lung_OC	lung:	n/a	n/a
46	CTCF	chr19:21784301-21784491	K562	blood:	n/a	n/a
47	CTCF	chr19:21782416-21782643	K562	blood:	n/a	n/a
48	CTCF	chr19:21784997-21785117	K562	blood:	n/a	n/a
49	CUX1	chr19:21784983-21785258	K562	blood:	n/a	n/a
50	CUX1	chr19:21784142-21784336	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:21773418-21773468	PrEC	prostate:	n/a
2	chr19:21767566-21767616	K562	blood:	n/a
3	chr19:21767566-21767616	HCPEpiC	choroid plexus:	n/a
4	chr19:21769190-21769240	GM12878	blood:	n/a
5	chr19:21769736-21769786	NB4	blood:	n/a
6	chr19:21773418-21773468	HCPEpiC	choroid plexus:	n/a
7	chr19:21769315-21769365	NHDF-neo	bronchial:	n/a
8	chr19:21769430-21769480	BE2_C	brain:	n/a
9	chr19:21769315-21769365	IMR90	lung:	fetal
10	chr19:21769315-21769365	ECC-1	luminal epithelium:	n/a
11	chr19:21769430-21769480	A549	lung:	n/a
12	chr19:21773418-21773468	Hepatocyte	liver:	n/a
13	chr19:21773418-21773468	NHBE	bronchial:	n/a
14	chr19:21769190-21769240	T-47D	breast:	n/a
15	chr19:21769430-21769480	AG10803	skin:	n/a
16	chr19:21769736-21769786	BJ	skin:	n/a
17	chr19:21769430-21769480	ECC-1	luminal epithelium:	n/a
18	chr19:21769430-21769480	HEK293	kidney:	embryo
19	chr19:21767566-21767616	NHDF-neo	bronchial:	n/a
20	chr19:21773418-21773468	NB4	blood:	n/a
21	chr19:21769736-21769786	GM12891	blood:	n/a
22	chr19:21769190-21769240	GM19239	blood:	n/a
23	chr19:21769736-21769786	LNCaP	prostate:	n/a
24	chr19:21767566-21767616	NB4	blood:	n/a
25	chr19:21773418-21773468	IMR90	lung:	fetal
26	chr19:21769190-21769240	HEEpiC	esophagus:	n/a
27	chr19:21769315-21769365	MCF10A-Er-Src	breast:	n/a
28	chr19:21769430-21769480	HMEC	breast:	n/a
29	chr19:21769430-21769480	AG04449	skin:	fetal
30	chr19:21769190-21769240	PrEC	prostate:	n/a
31	chr19:21769315-21769365	HCF	heart:	n/a
32	chr19:21769736-21769786	Hepatocyte	liver:	n/a
33	chr19:21769736-21769786	ProgFib	skin:	n/a
34	chr19:21773418-21773468	HMEC	breast:	n/a
35	chr19:21769190-21769240	AG04449	skin:	fetal
36	chr19:21769315-21769365	SK-N-SH_RA	brain:	n/a
37	chr19:21767566-21767616	Caco-2	colon:	n/a
38	chr19:21769190-21769240	K562	blood:	n/a
39	chr19:21769736-21769786	HNPCEpiC	eye:	n/a
40	chr19:21767566-21767616	AG10803	skin:	n/a
41	chr19:21769736-21769786	SAEC	small airway:	n/a
42	chr19:21769430-21769480	GM12891	blood:	n/a
43	chr19:21769430-21769480	LNCaP	prostate:	n/a
44	chr19:21769430-21769480	PrEC	prostate:	n/a
45	chr19:21769736-21769786	ovcar-3	ovarian:	n/a
46	chr19:21769315-21769365	PrEC	prostate:	n/a
47	chr19:21769430-21769480	ProgFib	skin:	n/a
48	chr19:21773418-21773468	LNCaP	prostate:	n/a
49	chr19:21769190-21769240	HUVEC	blood vessel:	n/a
50	chr19:21769315-21769365	HMEC	breast:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:21780063..21781970-chr19:21783251..21784988,3	K562	blood:
2	chr19:21776789..21778695-chr19:21784881..21786729,2	K562	blood:
3	chr19:21769231..21770804-chr19:21773382..21775361,2	K562	blood:
4	chr19:21784507..21786165-chr19:21795628..21798618,2	K562	blood:
5	chr19:21780063..21781970-chr19:21783251..21784988,3	K562	blood:
6	chr19:21759399..21762531-chr19:21766206..21768542,3	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF100-2	chr19:21769665-21770124	ENSG00000268555.1
2	lnc-ZNF100-1	chr19:21776487-21776720	ENSG00000268240.1
3	lnc-ZNF100-1	chr19:21777228-21777430	ENSG00000268240.1
4	lnc-ZNF100-2	chr19:21769665-21770045	ENSG00000249473
5	lnc-ZNF429-2	chr19:21780079-21780167	XLOC_013007
6	lnc-ZNF100-2	chr19:21769665-21770179	NONHSAT063726
7	lnc-ZNF100-1	chr19:21776485-21776704	NONHSAT063731
8	lnc-ZNF100-1	chr19:21770314-21770413	NONHSAT063731

No data

Variant related genes	Relation type
ENSG00000268240	TF binding region
ENSG00000268555	TF binding region
ENSG00000268240	CpG island
ENSG00000268555	CpG island
ENSG00000268240	chromatin interactions
ENSG00000268555	chromatin interactions

Extended variants
information (count: 874 )
Associated
traits (count: 42 )

Variant overlapped rSNPs/rCNVs (count:874 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577303099	chr19:21766636-21766637	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
2	rs34803660	chr19:21766669-21766670	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs112094901	chr19:21766677-21766678	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
4	rs184589119	chr19:21766686-21766687	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs530235574	chr19:21766696-21766697	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs549644703	chr19:21766701-21766702	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs76695906	chr19:21766710-21766711	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs200727596	chr19:21766719-21766720	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs564906158	chr19:21766747-21766748	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs73552446	chr19:21766756-21766757	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs200234320	chr19:21766757-21766758	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
12	rs188627956	chr19:21766766-21766767	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs371398679	chr19:21766772-21766773	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs377393282	chr19:21766774-21766775	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
15	rs7251673	chr19:21766786-21766787	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs368358648	chr19:21766816-21766817	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs116044227	chr19:21766819-21766820	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs143313381	chr19:21766831-21766832	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs546608546	chr19:21766838-21766839	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
20	rs200762038	chr19:21766868-21766869	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
21	rs148286502	chr19:21766870-21766871	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs571168551	chr19:21766881-21766882	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs551965710	chr19:21766885-21766886	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs532213860	chr19:21766921-21766922	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs141419604	chr19:21766929-21766930	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs74838491	chr19:21766950-21766951	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs12609183	chr19:21766970-21766971	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs148730068	chr19:21767058-21767059	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs142268643	chr19:21767119-21767120	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554902223	chr19:21767122-21767123	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs566789779	chr19:21767128-21767129	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs151019713	chr19:21767138-21767139	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558877967	chr19:21767158-21767159	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551816427	chr19:21767232-21767233	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs577192210	chr19:21767248-21767249	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs113387533	chr19:21767259-21767260	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371278404	chr19:21767281-21767282	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs574688724	chr19:21767311-21767312	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs534293570	chr19:21767354-21767355	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs372902136	chr19:21767369-21767370	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs112911979	chr19:21767380-21767381	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs373483704	chr19:21767422-21767423	Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs112204288	chr19:21767453-21767454	Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs554011474	chr19:21767469-21767470	Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs116454138	chr19:21767477-21767478	Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	mRNA abundance
46	rs75578524	chr19:21767520-21767521	Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs200586274	chr19:21767532-21767533	Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs564056462	chr19:21767586-21767587	Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs4809142	chr19:21767638-21767639	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs546199449	chr19:21767668-21767669	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:42)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:435 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21752000-21769600	Weak transcription	Fetal Heart	heart
2	chr19:21753000-21768000	Weak transcription	Fetal Intestine Small	intestine
3	chr19:21760200-21768000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr19:21760400-21769000	Weak transcription	Fetal Kidney	kidney
5	chr19:21762600-21766800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr19:21763400-21767200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr19:21763400-21767400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr19:21763400-21768000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr19:21764000-21767400	Weak transcription	Primary T cells from cord blood	blood
10	chr19:21764000-21767400	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr19:21764400-21767600	Enhancers	Primary T cells fromperipheralblood	blood
12	chr19:21764600-21768000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr19:21764800-21769000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr19:21765000-21767200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr19:21766200-21766800	Strong transcription	Fetal Intestine Large	intestine
16	chr19:21766200-21766800	ZNF genes & repeats	Left Ventricle	heart
17	chr19:21766200-21767000	Transcr. at gene 5' and 3'	Dnd41	blood
18	chr19:21766200-21770600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr19:21766600-21767600	Weak transcription	Pancreas	Pancrea
20	chr19:21766600-21768000	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr19:21766600-21768000	Weak transcription	Rectal Smooth Muscle	rectum
22	chr19:21766600-21769200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr19:21766800-21767000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr19:21766800-21767200	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr19:21766800-21768000	Weak transcription	Left Ventricle	heart
26	chr19:21766800-21768200	Weak transcription	Fetal Intestine Large	intestine
27	chr19:21767000-21767400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr19:21767000-21767400	Genic enhancers	Dnd41	blood
29	chr19:21767200-21767800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr19:21767200-21768800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr19:21767200-21768800	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr19:21767400-21767800	Enhancers	Thymus	Thymus
33	chr19:21767400-21768000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr19:21767400-21768600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr19:21767400-21768600	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
36	chr19:21767400-21768600	Transcr. at gene 5' and 3'	Dnd41	blood
37	chr19:21767400-21768800	Enhancers	Primary T cells from cord blood	blood
38	chr19:21767400-21768800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr19:21767400-21769000	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr19:21767600-21768000	Enhancers	Pancreas	Pancrea
41	chr19:21767600-21770800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
42	chr19:21767800-21768400	ZNF genes & repeats	Brain Substantia Nigra	brain
43	chr19:21767800-21768600	ZNF genes & repeats	Liver	Liver
44	chr19:21767800-21769000	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr19:21767800-21770800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr19:21767800-21771000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr19:21768000-21768200	Genic enhancers	Fetal Intestine Small	intestine
48	chr19:21768000-21768200	ZNF genes & repeats	Ovary	ovary
49	chr19:21768000-21768200	Flanking Active TSS	Pancreas	Pancrea
50	chr19:21768000-21768200	Enhancers	Stomach Mucosa	stomach

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