Variant report

Variant	esv3368478
Chromosome Location	chr4:6954301-6956199
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	BACH1	chr4:6955790-6956082	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr4:6955760-6956159	K562	blood:	n/a	n/a
3	CCNT2	chr4:6955676-6956057	K562	blood:	n/a	chr4:6955900-6955909
4	CEBPB	chr4:6955784-6955947	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr4:6955235-6955477	K562	blood:	n/a	n/a
6	CHD2	chr4:6955737-6956046	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr4:6955440-6955590	BE2_C	brain:	n/a	n/a
8	CTCF	chr4:6954789-6954841	Kidney_OC	kidney:	n/a	n/a
9	CTCF	chr4:6954740-6954890	RPTEC	kidney:	n/a	n/a
10	CTCF	chr4:6954720-6954870	RPTEC	kidney:	n/a	n/a
11	E2F4	chr4:6955689-6955984	MCF10A-Er-Src	breast:	n/a	chr4:6955838-6955848 chr4:6955841-6955851
12	E2F6	chr4:6955553-6956369	H1-hESC	embryonic stem cell:	n/a	chr4:6955838-6955848 chr4:6955841-6955851
13	E2F6	chr4:6955661-6956327	H1-hESC	embryonic stem cell:	n/a	chr4:6955838-6955848 chr4:6955841-6955851
14	E2F6	chr4:6955822-6956024	K562	blood:	n/a	chr4:6955838-6955848 chr4:6955841-6955851
15	E2F6	chr4:6955685-6956251	K562	blood:	n/a	chr4:6955838-6955848 chr4:6955841-6955851
16	E2F6	chr4:6955643-6956190	K562	blood:	n/a	chr4:6955838-6955848 chr4:6955841-6955851
17	EGR1	chr4:6955649-6956095	H1-hESC	embryonic stem cell:	n/a	chr4:6955832-6955842 chr4:6955841-6955851 chr4:6955842-6955853 chr4:6955836-6955858 chr4:6955842-6955851 chr4:6955841-6955854 chr4:6955840-6955854 chr4:6955841-6955854 chr4:6955840-6955855 chr4:6955841-6955854 chr4:6955841-6955854
18	EGR1	chr4:6955642-6956088	H1-hESC	embryonic stem cell:	n/a	chr4:6955832-6955842 chr4:6955841-6955851 chr4:6955842-6955853 chr4:6955836-6955858 chr4:6955842-6955851 chr4:6955841-6955854 chr4:6955840-6955854 chr4:6955841-6955854 chr4:6955840-6955855 chr4:6955841-6955854 chr4:6955841-6955854
19	EGR1	chr4:6955655-6955990	K562	blood:	n/a	chr4:6955832-6955842 chr4:6955841-6955851 chr4:6955842-6955853 chr4:6955836-6955858 chr4:6955842-6955851 chr4:6955841-6955854 chr4:6955840-6955854 chr4:6955841-6955854 chr4:6955840-6955855 chr4:6955841-6955854 chr4:6955841-6955854
20	EGR1	chr4:6955627-6956068	K562	blood:	n/a	chr4:6955832-6955842 chr4:6955841-6955851 chr4:6955842-6955853 chr4:6955836-6955858 chr4:6955842-6955851 chr4:6955841-6955854 chr4:6955840-6955854 chr4:6955841-6955854 chr4:6955840-6955855 chr4:6955841-6955854 chr4:6955841-6955854
21	EGR1	chr4:6955580-6956074	ECC-1	luminal epithelium:	n/a	chr4:6955832-6955842 chr4:6955841-6955851 chr4:6955842-6955853 chr4:6955836-6955858 chr4:6955842-6955851 chr4:6955841-6955854 chr4:6955840-6955854 chr4:6955841-6955854 chr4:6955840-6955855 chr4:6955841-6955854 chr4:6955841-6955854
22	EGR1	chr4:6955369-6956269	HCT-116	colon:	n/a	chr4:6955832-6955842 chr4:6955841-6955851 chr4:6955842-6955853 chr4:6955836-6955858 chr4:6955842-6955851 chr4:6955841-6955854 chr4:6955840-6955854 chr4:6955841-6955854 chr4:6955840-6955855 chr4:6955841-6955854 chr4:6955841-6955854
23	EGR1	chr4:6955565-6956153	ECC-1	luminal epithelium:	n/a	chr4:6955832-6955842 chr4:6955841-6955851 chr4:6955842-6955853 chr4:6955836-6955858 chr4:6955842-6955851 chr4:6955841-6955854 chr4:6955840-6955854 chr4:6955841-6955854 chr4:6955840-6955855 chr4:6955841-6955854 chr4:6955841-6955854
24	EGR1	chr4:6955318-6956274	HCT-116	colon:	n/a	chr4:6955832-6955842 chr4:6955841-6955851 chr4:6955842-6955853 chr4:6955836-6955858 chr4:6955842-6955851 chr4:6955841-6955854 chr4:6955840-6955854 chr4:6955841-6955854 chr4:6955840-6955855 chr4:6955841-6955854 chr4:6955841-6955854
25	ELF1	chr4:6955634-6955963	K562	blood:	n/a	chr4:6955839-6955851
26	EP300	chr4:6955821-6956053	K562	blood:	n/a	chr4:6955995-6956011
27	EP300	chr4:6955578-6956272	ECC-1	luminal epithelium:	n/a	chr4:6955995-6956011
28	FOS	chr4:6955363-6955923	MCF10A-Er-Src	breast:	n/a	chr4:6955525-6955533 chr4:6955526-6955537
29	FOS	chr4:6955508-6955707	MCF10A-Er-Src	breast:	n/a	chr4:6955525-6955533 chr4:6955526-6955537
30	FOS	chr4:6955467-6955710	MCF10A-Er-Src	breast:	n/a	chr4:6955525-6955533 chr4:6955526-6955537
31	FOS	chr4:6955484-6955932	MCF10A-Er-Src	breast:	n/a	chr4:6955525-6955533 chr4:6955526-6955537
32	GABPA	chr4:6955785-6956122	H1-hESC	embryonic stem cell:	n/a	n/a
33	GATA3	chr4:6955792-6956180	T-47D	breast:	n/a	n/a
34	GTF2F1	chr4:6955902-6956099	H1-hESC	embryonic stem cell:	n/a	n/a
35	HDAC2	chr4:6955481-6955629	K562	blood:	n/a	n/a
36	HMGN3	chr4:6955557-6956024	K562	blood:	n/a	n/a
37	JUND	chr4:6955680-6955946	K562	blood:	n/a	n/a
38	MAX	chr4:6955640-6956322	MCF-7	breast:	n/a	n/a
39	MAX	chr4:6955422-6956271	K562	blood:	n/a	n/a
40	MAX	chr4:6955683-6956214	K562	blood:	n/a	n/a
41	MAX	chr4:6955437-6956361	ECC-1	luminal epithelium:	n/a	n/a
42	MAX	chr4:6955693-6956213	SK-N-SH	brain:	n/a	n/a
43	MAX	chr4:6955625-6956102	K562	blood:	n/a	n/a
44	MAX	chr4:6955786-6956182	MCF-7	breast:	n/a	n/a
45	MAX	chr4:6955592-6956336	H1-hESC	embryonic stem cell:	n/a	n/a
46	MAX	chr4:6955574-6956269	H1-hESC	embryonic stem cell:	n/a	n/a
47	MAX	chr4:6955370-6956381	ECC-1	luminal epithelium:	n/a	n/a
48	MAX	chr4:6955710-6956206	HepG2	liver:	n/a	n/a
49	MAX	chr4:6955283-6956328	HCT-116	colon:	n/a	n/a
50	MAX	chr4:6955313-6956336	HCT-116	colon:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:6955953-6956003	GM12878	blood:	n/a
2	chr4:6955953-6956003	AoSMC	blood vessel:	n/a
3	chr4:6955953-6956003	SK-N-SH_RA	brain:	n/a
4	chr4:6955953-6956003	AG04450	lung:	fetal
5	chr4:6955698-6955748	RPTEC	kidney:	n/a
6	chr4:6955698-6955748	HPAEpiC	pulmonary alveolar:	n/a
7	chr4:6955698-6955748	HNPCEpiC	eye:	n/a
8	chr4:6955953-6956003	NT2-D1	testis:	n/a
9	chr4:6955953-6956003	A549	lung:	n/a
10	chr4:6955660-6955710	HRE	kidney:	n/a
11	chr4:6955953-6956003	PFSK-1	brain:	n/a
12	chr4:6955953-6956003	HCT-116	colon:	n/a
13	chr4:6955660-6955710	HNPCEpiC	eye:	n/a
14	chr4:6955660-6955710	SK-N-SH_RA	brain:	n/a
15	chr4:6955953-6956003	HUVEC	blood vessel:	n/a
16	chr4:6955660-6955710	PrEC	prostate:	n/a
17	chr4:6955660-6955710	NT2-D1	testis:	n/a
18	chr4:6955698-6955748	U87	brain:	n/a
19	chr4:6955698-6955748	AG04450	lung:	fetal
20	chr4:6955698-6955748	HAEpiC	amniotic membrane:	n/a
21	chr4:6955953-6956003	LNCaP	prostate:	n/a
22	chr4:6955698-6955748	BJ	skin:	n/a
23	chr4:6955698-6955748	Hela-S3	cervix:	n/a
24	chr4:6955698-6955748	AG04449	skin:	fetal
25	chr4:6955660-6955710	AG10803	skin:	n/a
26	chr4:6955953-6956003	HEK293	kidney:	embryo
27	chr4:6955698-6955748	SK-N-SH_RA	brain:	n/a
28	chr4:6955660-6955710	MCF-7	breast:	n/a
29	chr4:6955953-6956003	AG04449	skin:	fetal
30	chr4:6955953-6956003	AG09319	gingival:	n/a
31	chr4:6955660-6955710	LNCaP	prostate:	n/a
32	chr4:6955698-6955748	CMK	blood:	n/a
33	chr4:6955660-6955710	HEEpiC	esophagus:	n/a
34	chr4:6955698-6955748	PrEC	prostate:	n/a
35	chr4:6955953-6956003	PrEC	prostate:	n/a
36	chr4:6955953-6956003	HCF	heart:	n/a
37	chr4:6955953-6956003	Caco-2	colon:	n/a
38	chr4:6955953-6956003	GM06990	blood:	n/a
39	chr4:6955698-6955748	Caco-2	colon:	n/a
40	chr4:6955660-6955710	Hepatocyte	liver:	n/a
41	chr4:6955953-6956003	ovcar-3	ovarian:	n/a
42	chr4:6955953-6956003	Jurkat	blood:	n/a
43	chr4:6955660-6955710	T-47D	breast:	n/a
44	chr4:6955953-6956003	HRPEpiC	eye:	n/a
45	chr4:6955698-6955748	NT2-D1	testis:	n/a
46	chr4:6955660-6955710	AG04449	skin:	fetal
47	chr4:6955698-6955748	HEK293	kidney:	embryo
48	chr4:6955953-6956003	NB4	blood:	n/a
49	chr4:6955698-6955748	PFSK-1	brain:	n/a
50	chr4:6955698-6955748	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:6910837..6912550-chr4:6955221..6957525,2	MCF-7	breast:
2	chr4:6910740..6913101-chr4:6952369..6954537,2	K562	blood:

Variant related genes	Relation type
ENSG00000265953	TF binding region
TBC1D14	TF binding region
ENSG00000265953	CpG island
TBC1D14	CpG island
ENSG00000132405	chromatin interactions

Extended variants
information (count: 81 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:81 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542466950	chr4:6954306-6954307	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs371808134	chr4:6954322-6954323	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs529050021	chr4:6954374-6954375	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs550803352	chr4:6954383-6954384	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs34562748	chr4:6954390-6954391	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs569112718	chr4:6954425-6954426	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs185700770	chr4:6954430-6954431	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs572582139	chr4:6954468-6954469	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs575337186	chr4:6954507-6954508	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs566824557	chr4:6954535-6954536	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs56903115	chr4:6954564-6954565	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs555785935	chr4:6954567-6954568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138978102	chr4:6954573-6954574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs35490604	chr4:6954580-6954581	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs556338506	chr4:6954600-6954601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs577846628	chr4:6954613-6954614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564132364	chr4:6954626-6954627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560635280	chr4:6954648-6954649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs528058837	chr4:6954682-6954683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs149291507	chr4:6954693-6954694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs528043499	chr4:6954725-6954726	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs144565246	chr4:6954726-6954727	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs550741895	chr4:6954731-6954732	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs569050978	chr4:6954737-6954738	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs371101904	chr4:6954750-6954751	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs112342269	chr4:6954753-6954754	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs35819089	chr4:6954768-6954769	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs533177521	chr4:6954784-6954785	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs190947320	chr4:6954785-6954786	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs566659385	chr4:6954798-6954799	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs113004161	chr4:6954909-6954910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555470176	chr4:6954912-6954913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567371753	chr4:6954951-6954952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113072243	chr4:6955029-6955030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556276881	chr4:6955034-6955035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs375829742	chr4:6955070-6955071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369921641	chr4:6955074-6955075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs201183600	chr4:6955086-6955087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs76967305	chr4:6955098-6955099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs113513001	chr4:6955100-6955101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs79343136	chr4:6955103-6955104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs572657635	chr4:6955114-6955115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs80246016	chr4:6955121-6955122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550403012	chr4:6955127-6955128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568669413	chr4:6955128-6955129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs543344879	chr4:6955154-6955155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs377427393	chr4:6955200-6955201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs74591691	chr4:6955251-6955252	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs373627869	chr4:6955282-6955283	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs13133382	chr4:6955308-6955309	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	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
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	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
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD

Chromatin state (count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:6928000-6969600	Weak transcription	Aorta	Aorta
2	chr4:6943800-6955400	Weak transcription	Brain Substantia Nigra	brain
3	chr4:6944800-6955400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr4:6945000-6955400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr4:6945000-6970200	Weak transcription	Hela-S3	cervix
6	chr4:6945200-6955600	Weak transcription	Fetal Brain Female	brain
7	chr4:6945400-6955400	Weak transcription	Fetal Stomach	stomach
8	chr4:6945600-6955600	Weak transcription	Left Ventricle	heart
9	chr4:6945800-6965800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr4:6946400-6955400	Weak transcription	NHLF	lung
11	chr4:6946600-6955200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr4:6946600-6955400	Weak transcription	Stomach Smooth Muscle	stomach
13	chr4:6946600-6955800	Weak transcription	Fetal Brain Male	brain
14	chr4:6946600-6969000	Weak transcription	Dnd41	blood
15	chr4:6946800-6955400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr4:6946800-6955400	Weak transcription	Stomach Mucosa	stomach
17	chr4:6946800-6955400	Weak transcription	NHDF-Ad	bronchial
18	chr4:6947000-6955400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr4:6947000-6955600	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr4:6947200-6955400	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr4:6948600-6962400	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr4:6949800-6955800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr4:6950000-6955400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr4:6950200-6956600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr4:6950400-6955400	Weak transcription	Liver	Liver
26	chr4:6950400-6955400	Weak transcription	Colonic Mucosa	Colon
27	chr4:6950400-6955400	Weak transcription	Fetal Lung	lung
28	chr4:6950400-6955400	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr4:6950400-6955400	Weak transcription	HepG2	liver
30	chr4:6950400-6955600	Weak transcription	Pancreas	Pancrea
31	chr4:6950400-6963800	Weak transcription	Small Intestine	intestine
32	chr4:6952000-6954600	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr4:6952800-6954600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr4:6952800-6954800	Enhancers	Primary T cells fromperipheralblood	blood
35	chr4:6952800-6954800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr4:6952800-6954800	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr4:6952800-6955000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr4:6953000-6954400	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr4:6953000-6954400	Enhancers	Fetal Intestine Small	intestine
40	chr4:6953000-6954600	Enhancers	Primary B cells from peripheral blood	blood
41	chr4:6953000-6954600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
42	chr4:6953000-6954600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr4:6953200-6954400	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr4:6953200-6954600	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr4:6953400-6954400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr4:6953400-6954400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
47	chr4:6953400-6954600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr4:6953600-6954600	Enhancers	Duodenum Mucosa	Duodenum
49	chr4:6953600-6954600	Enhancers	GM12878-XiMat	blood
50	chr4:6953600-6954800	Enhancers	Primary monocytes fromperipheralblood	blood

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