Variant report

Variant	esv3414958
Chromosome Location	chr4:15704254-15708452
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:33)
CpG islands
(count:610)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:33 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr4:15704606-15704806	GM12878	blood:	n/a	n/a
2	BRCA1	chr4:15704827-15704863	GM12878	blood:	n/a	n/a
3	CEBPB	chr4:15704347-15704605	A549	lung:	n/a	n/a
4	CTCF	chr4:15705695-15705794	GM19239	blood:	n/a	n/a
5	CTCF	chr4:15704732-15704822	Spleen_OC	spleen:	n/a	n/a
6	CTCF	chr4:15704640-15704790	AG04449	skin:	n/a	n/a
7	E2F6	chr4:15704499-15705041	A549	lung:	n/a	n/a
8	ELF1	chr4:15704484-15704964	GM12878	blood:	n/a	n/a
9	JUND	chr4:15704542-15704952	A549	lung:	n/a	n/a
10	MAX	chr4:15704322-15705015	A549	lung:	n/a	n/a
11	MAX	chr4:15704322-15705025	A549	lung:	n/a	n/a
12	MAZ	chr4:15704661-15704853	GM12878	blood:	n/a	n/a
13	MYC	chr4:15705589-15705731	H1-hESC	embryonic stem cell:	n/a	n/a
14	MYC	chr4:15706027-15706138	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr4:15704670-15704835	SK-N-SH	brain:	n/a	n/a
16	POLR2A	chr4:15705613-15705868	HepG2	liver:	n/a	n/a
17	POLR2A	chr4:15704578-15704958	A549	lung:	n/a	n/a
18	POLR2A	chr4:15704618-15704918	A549	lung:	n/a	n/a
19	POLR2A	chr4:15706171-15706206	Gliobla	brain:	n/a	n/a
20	POLR2A	chr4:15704553-15704944	A549	lung:	n/a	n/a
21	POLR2A	chr4:15704557-15704838	HUVEC	blood vessel:	n/a	n/a
22	POLR2A	chr4:15704436-15705176	HL-60	blood:	n/a	n/a
23	POLR2A	chr4:15704439-15705084	HL-60	blood:	n/a	n/a
24	POLR2A	chr4:15704671-15704816	A549	lung:	n/a	n/a
25	POLR2A	chr4:15704512-15705015	HUVEC	blood vessel:	n/a	n/a
26	POLR2A	chr4:15704483-15704985	A549	lung:	n/a	n/a
27	POLR2A	chr4:15704695-15704892	IMR90	lung:	n/a	n/a
28	REST	chr4:15704119-15704308	SK-N-SH	brain:	n/a	chr4:15704259-15704279
29	REST	chr4:15704434-15705043	HL-60	blood:	n/a	n/a
30	SPI1	chr4:15704371-15705052	HL-60	blood:	n/a	chr4:15704718-15704731
31	SPI1	chr4:15704588-15704785	GM12878	blood:	n/a	chr4:15704718-15704731
32	TAF1	chr4:15704573-15704746	SK-N-SH	brain:	n/a	n/a
33	YY1	chr4:15704589-15704918	GM12878	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:15704429-15704479	SK-N-MC	brain:	n/a
2	chr4:15704550-15704600	ProgFib	skin:	n/a
3	chr4:15704599-15704649	T-47D	breast:	n/a
4	chr4:15708451-15708501	ovcar-3	ovarian:	n/a
5	chr4:15704680-15704730	AG04449	skin:	fetal
6	chr4:15706889-15706939	BJ	skin:	n/a
7	chr4:15708451-15708501	NHBE	bronchial:	n/a
8	chr4:15708451-15708501	RPTEC	kidney:	n/a
9	chr4:15704393-15704443	U87	brain:	n/a
10	chr4:15704429-15704479	HL-60	blood:	n/a
11	chr4:15704599-15704649	HMEC	breast:	n/a
12	chr4:15704599-15704649	HRPEpiC	eye:	n/a
13	chr4:15704680-15704730	HMEC	breast:	n/a
14	chr4:15704393-15704443	GM19239	blood:	n/a
15	chr4:15704680-15704730	GM12892	blood:	n/a
16	chr4:15704844-15704894	AG09319	gingival:	n/a
17	chr4:15704453-15704503	MCF10A-Er-Src	breast:	n/a
18	chr4:15704844-15704894	GM12878	blood:	n/a
19	chr4:15708451-15708501	T-47D	breast:	n/a
20	chr4:15704453-15704503	ECC-1	luminal epithelium:	n/a
21	chr4:15704680-15704730	Jurkat	blood:	n/a
22	chr4:15704393-15704443	GM12891	blood:	n/a
23	chr4:15704550-15704600	HUVEC	blood vessel:	n/a
24	chr4:15704453-15704503	PrEC	prostate:	n/a
25	chr4:15704599-15704649	NH-A	brain:	n/a
26	chr4:15706889-15706939	AoSMC	blood vessel:	n/a
27	chr4:15704429-15704479	U87	brain:	n/a
28	chr4:15704393-15704443	AG09309	skin:	n/a
29	chr4:15704393-15704443	PrEC	prostate:	n/a
30	chr4:15704795-15704845	IMR90	lung:	fetal
31	chr4:15704550-15704600	GM06990	blood:	n/a
32	chr4:15704680-15704730	HepG2	liver:	n/a
33	chr4:15706889-15706939	SK-N-MC	brain:	n/a
34	chr4:15704795-15704845	HCF	heart:	n/a
35	chr4:15704599-15704649	NHDF-neo	bronchial:	n/a
36	chr4:15704795-15704845	SK-N-SH	brain:	n/a
37	chr4:15708451-15708501	HepG2	liver:	n/a
38	chr4:15704393-15704443	LNCaP	prostate:	n/a
39	chr4:15704550-15704600	HCPEpiC	choroid plexus:	n/a
40	chr4:15704680-15704730	HNPCEpiC	eye:	n/a
41	chr4:15704680-15704730	PANC-1	pancreas:	n/a
42	chr4:15704453-15704503	HepG2	liver:	n/a
43	chr4:15704680-15704730	SAEC	small airway:	n/a
44	chr4:15704429-15704479	HEEpiC	esophagus:	n/a
45	chr4:15706889-15706939	HL-60	blood:	n/a
46	chr4:15704429-15704479	Jurkat	blood:	n/a
47	chr4:15704680-15704730	HRCEpiC	kidney:	n/a
48	chr4:15704550-15704600	SK-N-MC	brain:	n/a
49	chr4:15708451-15708501	HIPEpiC	eye:	n/a
50	chr4:15704453-15704503	GM12878	blood:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:15689195..15690724-chr4:15706537..15708519,2	K562	blood:
2	chr4:15697208..15699857-chr4:15706552..15708335,2	MCF-7	breast:
3	chr4:15655590..15657245-chr4:15703796..15706264,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM200B-1	chr4:15707138-15707188	NONHSAT095633

No data

Variant related genes	Relation type
BST1	TF binding region
BST1	CpG island
ENSG00000118564	chromatin interactions

Extended variants
information (count: 195 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:195 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs202049671	chr4:15704317-15704318	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs573043174	chr4:15704382-15704383	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs571697951	chr4:15704415-15704416	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs542066166	chr4:15704433-15704434	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs371748651	chr4:15704460-15704461	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs35606435	chr4:15704500-15704501	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs575067251	chr4:15704549-15704550	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs544018553	chr4:15704556-15704557	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs112044965	chr4:15704603-15704604	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs532497956	chr4:15704626-15704627	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs140592625	chr4:15704663-15704664	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs559740213	chr4:15704672-15704673	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs528488028	chr4:15704698-15704699	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs548819943	chr4:15704757-15704758	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs370174845	chr4:15704787-15704788	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs2302468	chr4:15704874-15704875	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs531107943	chr4:15704879-15704880	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs551222169	chr4:15704903-15704904	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs570556984	chr4:15704909-15704910	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs375955431	chr4:15704910-15704911	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs539558371	chr4:15704916-15704917	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs184852747	chr4:15704924-15704925	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs566416270	chr4:15704947-15704948	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs574160294	chr4:15704948-15704949	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs371380805	chr4:15704972-15704973	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs555208527	chr4:15705012-15705013	Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs2302467	chr4:15705039-15705040	Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs563451565	chr4:15705053-15705054	Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs557579640	chr4:15705134-15705135	Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs532254973	chr4:15705142-15705143	Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs115890946	chr4:15705162-15705163	Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs200430877	chr4:15705185-15705186	Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs546240618	chr4:15705192-15705193	Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs559597234	chr4:15705198-15705199	Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs552439912	chr4:15705200-15705201	Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs528462308	chr4:15705217-15705218	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs189310075	chr4:15705235-15705236	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs201773479	chr4:15705252-15705253	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs545560006	chr4:15705254-15705255	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs76422069	chr4:15705256-15705257	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs559033385	chr4:15705265-15705266	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs138333020	chr4:15705267-15705268	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs78739477	chr4:15705268-15705269	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs112033687	chr4:15705269-15705270	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs74346571	chr4:15705270-15705271	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs111928951	chr4:15705271-15705272	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs571014602	chr4:15705272-15705273	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs371100446	chr4:15705326-15705327	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs533363864	chr4:15705332-15705333	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs140146676	chr4:15705337-15705338	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:49)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:320 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:15684000-15704400	Weak transcription	Left Ventricle	heart
2	chr4:15684800-15704400	Weak transcription	Aorta	Aorta
3	chr4:15686600-15704400	Weak transcription	Thymus	Thymus
4	chr4:15697600-15704400	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr4:15697600-15723600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:15702600-15704400	Enhancers	Liver	Liver
7	chr4:15703200-15704600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
8	chr4:15703200-15706600	Weak transcription	HepG2	liver
9	chr4:15703600-15704400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr4:15703800-15704400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:15703800-15704400	Enhancers	Brain Substantia Nigra	brain
12	chr4:15703800-15704600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr4:15703800-15704600	Enhancers	Fetal Heart	heart
14	chr4:15703800-15704800	Flanking Active TSS	Primary B cells from cord blood	blood
15	chr4:15703800-15705400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
16	chr4:15703800-15705600	Active TSS	Stomach Smooth Muscle	stomach
17	chr4:15704000-15704400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr4:15704000-15704400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr4:15704000-15704400	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr4:15704000-15704400	Flanking Active TSS	Primary T cells from cord blood	blood
21	chr4:15704000-15704400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
22	chr4:15704000-15704400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr4:15704000-15704400	Enhancers	Primary T helper naive cells from peripheral blood	blood
24	chr4:15704000-15704400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr4:15704000-15704400	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr4:15704000-15704400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr4:15704000-15704400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr4:15704000-15704400	Enhancers	Muscle Satellite Cultured Cells	--
29	chr4:15704000-15704400	Enhancers	Brain Angular Gyrus	brain
30	chr4:15704000-15704400	Enhancers	Brain Anterior Caudate	brain
31	chr4:15704000-15704400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr4:15704000-15704400	Enhancers	Colon Smooth Muscle	Colon
33	chr4:15704000-15704400	Flanking Active TSS	Duodenum Mucosa	Duodenum
34	chr4:15704000-15704400	Enhancers	Duodenum Smooth Muscle	Duodenum
35	chr4:15704000-15704400	Flanking Active TSS	Fetal Intestine Large	intestine
36	chr4:15704000-15704400	Enhancers	Placenta	Placenta
37	chr4:15704000-15704400	Enhancers	Right Atrium	heart
38	chr4:15704000-15704400	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr4:15704000-15704400	Flanking Active TSS	Dnd41	blood
40	chr4:15704000-15704400	Enhancers	HUVEC	blood vessel
41	chr4:15704000-15704600	Flanking Active TSS	Primary hematopoietic stem cells	blood
42	chr4:15704000-15704600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr4:15704000-15704600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr4:15704000-15704600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
45	chr4:15704000-15704600	Flanking Active TSS	Fetal Intestine Small	intestine
46	chr4:15704000-15704600	Enhancers	Gastric	stomach
47	chr4:15704000-15704600	Enhancers	Lung	lung
48	chr4:15704000-15704600	Enhancers	Sigmoid Colon	Sigmoid Colon
49	chr4:15704000-15704600	Enhancers	Stomach Mucosa	stomach
50	chr4:15704000-15704600	Flanking Active TSS	NHEK	skin

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