Variant report

Variant	esv3437338
Chromosome Location	chr4:1220202-1222700
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:77)
CpG islands
(count:550)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:77 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr4:1221264-1221330	GM19239	blood:	n/a	n/a
2	CTCF	chr4:1221267-1221395	GM12891	blood:	n/a	n/a
3	CTCF	chr4:1221088-1221233	GM19239	blood:	n/a	n/a
4	CTCF	chr4:1221172-1221251	GM12891	blood:	n/a	n/a
5	MAFK	chr4:1221415-1221521	HepG2	liver:	n/a	n/a
6	MAX	chr4:1221699-1221933	NB4	blood:	n/a	n/a
7	MAX	chr4:1220862-1221170	NB4	blood:	n/a	chr4:1221049-1221059 chr4:1221020-1221030
8	MYC	chr4:1221285-1221310	MCF-7	breast:	n/a	n/a
9	MYC	chr4:1221827-1221915	NB4	blood:	n/a	n/a
10	MYC	chr4:1221062-1221156	GM12878	blood:	n/a	n/a
11	NR2C2	chr4:1221000-1221621	GM12878	blood:	n/a	n/a
12	POLR2A	chr4:1220852-1221607	GM12891	blood:	n/a	n/a
13	POLR2A	chr4:1221045-1221632	ECC-1	luminal epithelium:	n/a	n/a
14	POLR2A	chr4:1222512-1222784	GM12878	blood:	n/a	n/a
15	POLR2A	chr4:1220858-1221532	K562	blood:	n/a	n/a
16	POLR2A	chr4:1221084-1221283	U87	brain:	n/a	n/a
17	POLR2A	chr4:1222381-1223690	ECC-1	luminal epithelium:	n/a	n/a
18	POLR2A	chr4:1222556-1222784	K562	blood:	n/a	n/a
19	POLR2A	chr4:1222023-1222052	HepG2	liver:	n/a	n/a
20	POLR2A	chr4:1221948-1221969	HepG2	liver:	n/a	n/a
21	POLR2A	chr4:1220811-1221679	GM12878	blood:	n/a	n/a
22	POLR2A	chr4:1220969-1221659	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr4:1221549-1221557	MCF-7	breast:	n/a	n/a
24	POLR2A	chr4:1221218-1221401	MCF-7	breast:	n/a	n/a
25	POLR2A	chr4:1221270-1221541	Hela-S3	cervix:	n/a	n/a
26	POLR2A	chr4:1221098-1221540	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr4:1221995-1221999	HepG2	liver:	n/a	n/a
28	POLR2A	chr4:1220832-1221542	HepG2	liver:	n/a	n/a
29	POLR2A	chr4:1221163-1222120	HL-60	blood:	n/a	n/a
30	POLR2A	chr4:1220813-1221604	GM12892	blood:	n/a	n/a
31	POLR2A	chr4:1222640-1223976	GM12892	blood:	n/a	n/a
32	POLR2A	chr4:1220840-1221676	GM12878	blood:	n/a	n/a
33	POLR2A	chr4:1220934-1221111	GM12878	blood:	n/a	n/a
34	POLR2A	chr4:1221160-1221401	MCF-7	breast:	n/a	n/a
35	POLR2A	chr4:1221032-1221081	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr4:1221334-1222064	HL-60	blood:	n/a	n/a
37	POLR2A	chr4:1220310-1224704	K562	blood:	n/a	n/a
38	POLR2A	chr4:1221277-1221638	GM12878	blood:	n/a	n/a
39	POLR2A	chr4:1221044-1221266	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr4:1221408-1221438	MCF-7	breast:	n/a	n/a
41	POLR2A	chr4:1222228-1222731	HepG2	liver:	n/a	n/a
42	POLR2A	chr4:1220807-1221663	SK-N-MC	brain:	n/a	n/a
43	POLR2A	chr4:1219909-1220301	K562	blood:	n/a	n/a
44	POLR2A	chr4:1220876-1221173	K562	blood:	n/a	n/a
45	POLR2A	chr4:1221537-1221726	K562	blood:	n/a	n/a
46	POLR2A	chr4:1221402-1221403	MCF-7	breast:	n/a	n/a
47	POLR2A	chr4:1221338-1221736	U87	brain:	n/a	n/a
48	POLR2A	chr4:1220859-1221100	GM12878	blood:	n/a	n/a
49	POLR2A	chr4:1221137-1221425	ProgFib	skin:	n/a	n/a
50	POLR2A	chr4:1222157-1222476	K562	blood:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1222382-1222432	ProgFib	skin:	n/a
2	chr4:1222382-1222432	ProgFib	skin:	n/a
3	chr4:1221838-1221888	HCT-116	colon:	n/a
4	chr4:1221935-1221985	H1-hESC	embryonic stem cell:	embryo
5	chr4:1222037-1222087	HCM	heart:	n/a
6	chr4:1222382-1222432	HCM	heart:	n/a
7	chr4:1221935-1221985	K562	blood:	n/a
8	chr4:1222440-1222490	MCF-7	breast:	n/a
9	chr4:1222621-1222671	AG09309	skin:	n/a
10	chr4:1222382-1222432	HRCEpiC	kidney:	n/a
11	chr4:1221935-1221985	GM12891	blood:	n/a
12	chr4:1220556-1220606	NT2-D1	testis:	n/a
13	chr4:1222292-1222342	A549	lung:	n/a
14	chr4:1221838-1221888	SKMC	muscle:	n/a
15	chr4:1221935-1221985	HEK293	kidney:	embryo
16	chr4:1220951-1221001	HCT-116	colon:	n/a
17	chr4:1222292-1222342	HepG2	liver:	n/a
18	chr4:1220951-1221001	K562	blood:	n/a
19	chr4:1220556-1220606	GM19239	blood:	n/a
20	chr4:1222037-1222087	HMEC	breast:	n/a
21	chr4:1222440-1222490	HRCEpiC	kidney:	n/a
22	chr4:1222292-1222342	HRE	kidney:	n/a
23	chr4:1220556-1220606	HCT-116	colon:	n/a
24	chr4:1222440-1222490	SK-N-SH	brain:	n/a
25	chr4:1222440-1222490	CMK	blood:	n/a
26	chr4:1222037-1222087	HCPEpiC	choroid plexus:	n/a
27	chr4:1222037-1222087	ovcar-3	ovarian:	n/a
28	chr4:1220951-1221001	Caco-2	colon:	n/a
29	chr4:1221935-1221985	HAEpiC	amniotic membrane:	n/a
30	chr4:1222440-1222490	AG04449	skin:	fetal
31	chr4:1222292-1222342	HRPEpiC	eye:	n/a
32	chr4:1221935-1221985	SAEC	small airway:	n/a
33	chr4:1221838-1221888	NT2-D1	testis:	n/a
34	chr4:1221838-1221888	GM12878	blood:	n/a
35	chr4:1222621-1222671	HCPEpiC	choroid plexus:	n/a
36	chr4:1221935-1221985	HUVEC	blood vessel:	n/a
37	chr4:1221838-1221888	MCF10A-Er-Src	breast:	n/a
38	chr4:1221935-1221985	SK-N-SH_RA	brain:	n/a
39	chr4:1220556-1220606	HRPEpiC	eye:	n/a
40	chr4:1222621-1222671	AG04449	skin:	fetal
41	chr4:1220951-1221001	HUVEC	blood vessel:	n/a
42	chr4:1222292-1222342	HIPEpiC	eye:	n/a
43	chr4:1222292-1222342	NHDF-neo	bronchial:	n/a
44	chr4:1220556-1220606	HRCEpiC	kidney:	n/a
45	chr4:1222292-1222342	LNCaP	prostate:	n/a
46	chr4:1222037-1222087	GM12878	blood:	n/a
47	chr4:1220556-1220606	HUVEC	blood vessel:	n/a
48	chr4:1222292-1222342	HAEpiC	amniotic membrane:	n/a
49	chr4:1220556-1220606	U87	brain:	n/a
50	chr4:1222440-1222490	K562	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:1215883..1221793-chr4:1233494..1238232,6	K562	blood:
2	chr4:1219143..1221497-chr4:1224349..1226849,2	MCF-7	breast:
3	chr4:1221651..1224397-chr4:1224479..1227066,2	MCF-7	breast:
4	chr4:1218830..1221524-chr4:1242783..1244802,2	MCF-7	breast:
5	chr4:1216435..1221821-chr4:1240439..1244617,5	MCF-7	breast:
6	chr4:1222400..1224285-chr4:1225598..1228756,4	MCF-7	breast:
7	chr4:1209494..1211546-chr4:1218177..1220594,3	MCF-7	breast:
8	chr4:1215555..1220351-chr4:1239288..1242893,7	K562	blood:
9	chr4:1195937..1198894-chr4:1221468..1224458,3	K562	blood:

No data

Variant related genes	Relation type
CTBP1	TF binding region
CTBP1	CpG island
ENSG00000159674	chromatin interactions
ENSG00000196810	chromatin interactions
ENSG00000159692	chromatin interactions

Extended variants
information (count: 179 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:179 , 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	rs3775104	chr4:1220215-1220216	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557492978	chr4:1220223-1220224	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs1680057	chr4:1220244-1220245	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs538156450	chr4:1220245-1220246	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs556289460	chr4:1220283-1220284	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs561336293	chr4:1220297-1220298	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs574735692	chr4:1220298-1220299	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs535566963	chr4:1220317-1220318	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs114854368	chr4:1220326-1220327	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs377018731	chr4:1220357-1220358	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs546151065	chr4:1220372-1220373	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs183888628	chr4:1220378-1220379	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs150518674	chr4:1220393-1220394	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs554312120	chr4:1220408-1220409	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs543787357	chr4:1220410-1220411	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs561857138	chr4:1220430-1220431	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs139457729	chr4:1220432-1220433	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs111628519	chr4:1220447-1220448	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs547157560	chr4:1220448-1220449	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs559373390	chr4:1220525-1220526	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs372597705	chr4:1220535-1220536	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs532904402	chr4:1220554-1220555	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs551313316	chr4:1220557-1220558	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs542992911	chr4:1220576-1220577	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs1680056	chr4:1220583-1220584	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs538144319	chr4:1220588-1220589	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs550100539	chr4:1220596-1220597	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs1680055	chr4:1220603-1220604	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs568299260	chr4:1220611-1220612	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs536074567	chr4:1220617-1220618	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs188782942	chr4:1220661-1220662	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs572463379	chr4:1220671-1220672	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs75777974	chr4:1220680-1220681	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs558180789	chr4:1220681-1220682	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs576547949	chr4:1220687-1220688	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs543726579	chr4:1220688-1220689	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs193050193	chr4:1220691-1220692	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs73793138	chr4:1220692-1220693	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs541188855	chr4:1220702-1220703	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs547060513	chr4:1220708-1220709	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs111808830	chr4:1220755-1220756	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs532994483	chr4:1220825-1220826	Strong transcription Genic enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs551106590	chr4:1220826-1220827	Strong transcription Genic enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs75329749	chr4:1220862-1220863	Strong transcription Genic enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs530457109	chr4:1220876-1220877	Strong transcription Genic enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs188473662	chr4:1220887-1220888	Strong transcription Genic enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs373155897	chr4:1220906-1220907	Strong transcription Genic enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs116590995	chr4:1220919-1220920	Strong transcription Genic enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs559024283	chr4:1220938-1220939	Strong transcription Genic enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs547923434	chr4:1220951-1220952	Strong transcription Genic enhancers ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
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
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	20932292	CNVD
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20393555	CNVD

Chromatin state (count:213 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1203800-1223000	Strong transcription	Osteobl	bone
2	chr4:1204400-1227200	Strong transcription	Fetal Intestine Small	intestine
3	chr4:1204400-1235800	Strong transcription	HUES6 Cell Line	embryonic stem cell
4	chr4:1204600-1220400	Strong transcription	Liver	Liver
5	chr4:1204600-1236200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:1204800-1226400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:1204800-1237000	Weak transcription	Psoas Muscle	Psoas
8	chr4:1205000-1226200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr4:1205400-1226800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr4:1205800-1228200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr4:1206000-1226800	Strong transcription	Fetal Brain Female	brain
12	chr4:1206400-1226800	Strong transcription	Brain Germinal Matrix	brain
13	chr4:1206600-1227600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr4:1208800-1228000	Strong transcription	Muscle Satellite Cultured Cells	--
15	chr4:1210600-1225200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr4:1211400-1235400	Weak transcription	Small Intestine	intestine
17	chr4:1211600-1235400	Strong transcription	Sigmoid Colon	Sigmoid Colon
18	chr4:1212600-1225200	Strong transcription	Fetal Muscle Leg	muscle
19	chr4:1212600-1237000	Strong transcription	Dnd41	blood
20	chr4:1213600-1224200	Strong transcription	Placenta	Placenta
21	chr4:1213800-1221800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr4:1214200-1221200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr4:1214200-1221600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr4:1214200-1235600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr4:1214200-1236800	Strong transcription	Primary T cells from cord blood	blood
26	chr4:1214400-1222200	Strong transcription	Brain Cingulate Gyrus	brain
27	chr4:1214400-1222200	Strong transcription	Brain Inferior Temporal Lobe	brain
28	chr4:1214400-1225000	Strong transcription	Brain Hippocampus Middle	brain
29	chr4:1214400-1225600	Strong transcription	Aorta	Aorta
30	chr4:1214400-1235200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr4:1214400-1235600	Strong transcription	H1 Cell Line	embryonic stem cell
32	chr4:1214400-1236400	Strong transcription	Primary neutrophils fromperipheralblood	blood
33	chr4:1214400-1238400	Strong transcription	Thymus	Thymus
34	chr4:1214600-1225400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr4:1214600-1226400	Strong transcription	Cortex derived primary cultured neurospheres	brain
36	chr4:1214600-1227400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr4:1214600-1227600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr4:1214600-1235800	Strong transcription	Primary T helper cells fromperipheralblood	blood
39	chr4:1214600-1236200	Strong transcription	Monocytes-CD14+_RO01746	blood
40	chr4:1215000-1220800	Strong transcription	Skeletal Muscle Female	skeletal muscle
41	chr4:1215000-1226800	Strong transcription	Colonic Mucosa	Colon
42	chr4:1215000-1235200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr4:1215000-1236000	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr4:1215400-1221000	Strong transcription	Brain Substantia Nigra	brain
45	chr4:1215400-1225800	Strong transcription	Brain Anterior Caudate	brain
46	chr4:1215400-1226600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr4:1215400-1236000	Strong transcription	Primary B cells from peripheral blood	blood
48	chr4:1215800-1226600	Strong transcription	Fetal Stomach	stomach
49	chr4:1215800-1235600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr4:1216400-1227800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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