Variant report

Variant	esv2763527
Chromosome Location	chr6:2390712-2400244
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:97)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:34)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:97 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr6:2397163-2397489	IMR90	lung:	n/a	n/a
2	CEBPB	chr6:2391185-2391281	K562	blood:	n/a	chr6:2391223-2391234
3	CEBPB	chr6:2391111-2391311	A549	lung:	n/a	chr6:2391223-2391234
4	CEBPB	chr6:2391114-2391346	HepG2	liver:	n/a	chr6:2391223-2391234
5	CEBPB	chr6:2391113-2391366	IMR90	lung:	n/a	chr6:2391223-2391234
6	CTCF	chr6:2396718-2396741	GM13976	blood:	n/a	n/a
7	CTCF	chr6:2397360-2397510	AG09309	skin:	n/a	n/a
8	CTCF	chr6:2396688-2396802	GM12878	blood:	n/a	n/a
9	CTCF	chr6:2396629-2396831	IMR90	lung:	n/a	n/a
10	CTCF	chr6:2396620-2396770	WERI-Rb-1	eye:	n/a	n/a
11	CTCF	chr6:2396700-2396850	AG09319	gingival:	n/a	n/a
12	CTCF	chr6:2396620-2396770	NHEK	skin:	n/a	n/a
13	CTCF	chr6:2396720-2396870	HPF	lung:	n/a	n/a
14	CTCF	chr6:2396720-2396870	HCPEpiC	choroid plexus:	n/a	n/a
15	CTCF	chr6:2396720-2396870	HAc	cerebellar:	n/a	n/a
16	CTCF	chr6:2396680-2396830	HRPEpiC	eye:	n/a	n/a
17	CTCF	chr6:2396600-2396750	GM12872	blood:	n/a	n/a
18	CTCF	chr6:2396640-2396790	AG04450	lung:	n/a	n/a
19	CTCF	chr6:2397380-2397530	BJ	skin:	n/a	n/a
20	CTCF	chr6:2396580-2396730	Caco-2	colon:	n/a	n/a
21	CTCF	chr6:2396641-2396814	HepG2	liver:	n/a	n/a
22	CTCF	chr6:2396660-2396810	HCFaa	heart:	n/a	n/a
23	CTCF	chr6:2396700-2396850	HFF-Myc	foreskin:	n/a	n/a
24	CTCF	chr6:2396560-2396710	HMF	breast:	n/a	n/a
25	CTCF	chr6:2396681-2396824	MCF-7	breast:	n/a	n/a
26	CTCF	chr6:2397460-2397610	NHDF-neo	bronchial:	n/a	n/a
27	CTCF	chr6:2398540-2398690	AG04449	skin:	n/a	n/a
28	CTCF	chr6:2396740-2396890	AG09309	skin:	n/a	n/a
29	CTCF	chr6:2397340-2397490	AG09319	gingival:	n/a	n/a
30	CTCF	chr6:2397280-2397430	HPF	lung:	n/a	n/a
31	CTCF	chr6:2397180-2397330	GM12869	blood:	n/a	n/a
32	CTCF	chr6:2396700-2396850	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr6:2396660-2396810	AG10803	skin:	n/a	n/a
34	CTCF	chr6:2396684-2396790	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr6:2396540-2396690	AG09309	skin:	n/a	n/a
36	CTCF	chr6:2396661-2396797	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr6:2396660-2396810	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr6:2396680-2396830	NHLF	lung:	n/a	n/a
39	CTCF	chr6:2396652-2396803	HepG2	liver:	n/a	n/a
40	CTCF	chr6:2396780-2396930	HFF	foreskin:	n/a	n/a
41	CTCF	chr6:2396580-2396730	HepG2	liver:	n/a	n/a
42	CTCF	chr6:2394520-2394670	A549	lung:	n/a	n/a
43	CTCF	chr6:2396680-2396830	AG04449	skin:	n/a	n/a
44	CTCF	chr6:2396640-2396790	A549	lung:	n/a	n/a
45	CTCF	chr6:2397280-2397430	HFF	foreskin:	n/a	n/a
46	CTCF	chr6:2396680-2396830	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr6:2396668-2396821	LNCaP	prostate:	n/a	n/a
48	CTCF	chr6:2396665-2396805	LNCaP	prostate:	n/a	n/a
49	CTCF	chr6:2396680-2396830	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr6:2396654-2396832	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:2397671-2397721	NHDF-neo	bronchial:	n/a
2	chr6:2397671-2397721	GM12878	blood:	n/a
3	chr6:2397671-2397721	AG09319	gingival:	n/a
4	chr6:2397671-2397721	Hepatocyte	liver:	n/a
5	chr6:2397671-2397721	AG09309	skin:	n/a
6	chr6:2397671-2397721	PANC-1	pancreas:	n/a
7	chr6:2397671-2397721	LNCaP	prostate:	n/a
8	chr6:2397671-2397721	ProgFib	skin:	n/a
9	chr6:2397671-2397721	BJ	skin:	n/a
10	chr6:2397671-2397721	IMR90	lung:	fetal
11	chr6:2397671-2397721	HPAEpiC	pulmonary alveolar:	n/a
12	chr6:2397671-2397721	HCF	heart:	n/a
13	chr6:2397671-2397721	K562	blood:	n/a
14	chr6:2397671-2397721	HRCEpiC	kidney:	n/a
15	chr6:2397671-2397721	GM12892	blood:	n/a
16	chr6:2397671-2397721	HEEpiC	esophagus:	n/a
17	chr6:2397671-2397721	HMEC	breast:	n/a
18	chr6:2397671-2397721	NT2-D1	testis:	n/a
19	chr6:2397671-2397721	T-47D	breast:	n/a
20	chr6:2397671-2397721	HCT-116	colon:	n/a
21	chr6:2397671-2397721	NH-A	brain:	n/a
22	chr6:2397671-2397721	HCM	heart:	n/a
23	chr6:2397671-2397721	HUVEC	blood vessel:	n/a
24	chr6:2397671-2397721	HRPEpiC	eye:	n/a
25	chr6:2397671-2397721	Caco-2	colon:	n/a
26	chr6:2397671-2397721	SAEC	small airway:	n/a
27	chr6:2397671-2397721	MCF-7	breast:	n/a
28	chr6:2397671-2397721	SK-N-SH	brain:	n/a
29	chr6:2397671-2397721	HCPEpiC	choroid plexus:	n/a
30	chr6:2397671-2397721	SKMC	muscle:	n/a
31	chr6:2397671-2397721	Hela-S3	cervix:	n/a
32	chr6:2397671-2397721	AG04449	skin:	fetal
33	chr6:2397671-2397721	RPTEC	kidney:	n/a
34	chr6:2397671-2397721	BE2_C	brain:	n/a
35	chr6:2397671-2397721	HEK293	kidney:	embryo
36	chr6:2397671-2397721	HRE	kidney:	n/a
37	chr6:2397671-2397721	NHBE	bronchial:	n/a
38	chr6:2397671-2397721	AG10803	skin:	n/a
39	chr6:2397671-2397721	A549	lung:	n/a
40	chr6:2397671-2397721	GM19239	blood:	n/a
41	chr6:2397671-2397721	U87	brain:	n/a
42	chr6:2397671-2397721	MCF10A-Er-Src	breast:	n/a
43	chr6:2397671-2397721	NB4	blood:	n/a
44	chr6:2397671-2397721	HL-60	blood:	n/a
45	chr6:2397671-2397721	HNPCEpiC	eye:	n/a
46	chr6:2397671-2397721	AG04450	lung:	fetal
47	chr6:2397671-2397721	GM12891	blood:	n/a
48	chr6:2397671-2397721	H1-hESC	embryonic stem cell:	embryo
49	chr6:2397671-2397721	SK-N-SH_RA	brain:	n/a
50	chr6:2397671-2397721	AoSMC	blood vessel:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:2382708..2384223-chr6:2394952..2397063,2	MCF-7	breast:
2	chr6:1596675..1597218-chr6:2396217..2396777,2	K562	blood:
3	chr6:2362511..2364691-chr6:2394137..2395852,2	MCF-7	breast:
4	chr6:2396597..2398652-chr6:2400293..2401857,2	K562	blood:
5	chr6:1596186..1596789-chr6:2396672..2397233,2	MCF-7	breast:

(count:34 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WRNIP1-2	chr6:2398811-2398981	ENSG00000250903
2	lnc-WRNIP1-2	chr6:2399197-2399254	ucscGeneNc_uc003mtu_1
3	lnc-WRNIP1-2	chr6:2399241-2399271	NONHSAT106664
4	lnc-WRNIP1-2	chr6:2399100-2399271	XLOC_005127
5	lnc-WRNIP1-2	chr6:2397455-2397860	ENSG00000250903
6	lnc-WRNIP1-2	chr6:2398891-2399012	ENSG00000250903.4
7	lnc-WRNIP1-2	chr6:2397580-2397860	NONHSAT106659
8	lnc-WRNIP1-2	chr6:2399117-2399235	ENSG00000250903
9	lnc-WRNIP1-2	chr6:2398811-2399012	ENSG00000250903.4
10	lnc-WRNIP1-2	chr6:2398809-2399012	ENSG00000250903
11	lnc-WRNIP1-2	chr6:2398811-2399012	NONHSAT106620
12	lnc-WRNIP1-2	chr6:2398806-2399012	XLOC_005127
13	lnc-WRNIP1-2	chr6:2399100-2399271	ENSG00000250903.4
14	lnc-WRNIP1-2	chr6:2398811-2399012	ENSG00000250903
15	lnc-WRNIP1-2	chr6:2397455-2397754	NONHSAT106637
16	lnc-WRNIP1-2	chr6:2399100-2399271	ENSG00000250903.4
17	lnc-WRNIP1-2	chr6:2399100-2399271	NONHSAT106620
18	lnc-WRNIP1-2	chr6:2398811-2399012	NONHSAT106659
19	lnc-WRNIP1-2	chr6:2398811-2399012	XLOC_005127
20	lnc-WRNIP1-2	chr6:2397455-2397580	ENSG00000250903
21	lnc-WRNIP1-2	chr6:2399100-2399271	NONHSAT106659
22	lnc-WRNIP1-2	chr6:2398209-2398535	XLOC_005127
23	lnc-WRNIP1-2	chr6:2397477-2397860	XLOC_005127
24	lnc-WRNIP1-2	chr6:2399117-2399271	XLOC_005127
25	lnc-WRNIP1-2	chr6:2399100-2399271	XLOC_005127
26	lnc-WRNIP1-2	chr6:2398811-2399012	XLOC_005127
27	lnc-WRNIP1-2	chr6:2399117-2399226	XLOC_005127
28	lnc-WRNIP1-2	chr6:2398823-2399012	XLOC_005127
29	lnc-WRNIP1-2	chr6:2399216-2399271	XLOC_005127
30	lnc-WRNIP1-2	chr6:2399216-2399271	XLOC_005127
31	lnc-WRNIP1-2	chr6:2398811-2398857	NONHSAT106627
32	lnc-WRNIP1-2	chr6:2399100-2399271	ENSG00000250903
33	lnc-WRNIP1-2	chr6:2399100-2399271	XLOC_005127
34	lnc-WRNIP1-2	chr6:2398811-2399000	ENSG00000250903

No data

Variant related genes	Relation type
GMDS-AS1	TF binding region
GMDS-AS1	CpG island
PLAGL2	miRNA target sites
SPG20	miRNA target sites
CLEC4D	miRNA target sites
KIF5A	miRNA target sites
TMED10	miRNA target sites
TMEM194A	miRNA target sites
BTBD3	miRNA target sites
SMARCE1	miRNA target sites
PDE4D	miRNA target sites

Extended variants
information (count: 371 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:371 , 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	rs17134987	chr6:2390712-2390713	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs114088729	chr6:2390732-2390733	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs576097962	chr6:2390747-2390748	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs564641568	chr6:2390810-2390811	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs561686374	chr6:2390812-2390813	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs59455919	chr6:2390842-2390843	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs140300109	chr6:2390877-2390878	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564409762	chr6:2390927-2390928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144250842	chr6:2390970-2390971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs527547018	chr6:2391011-2391012	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564984363	chr6:2391029-2391030	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs367644735	chr6:2391046-2391047	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145454855	chr6:2391061-2391062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531660130	chr6:2391067-2391068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548682035	chr6:2391136-2391137	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs568524232	chr6:2391159-2391160	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs563033266	chr6:2391250-2391251	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs199796871	chr6:2391254-2391255	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs34173931	chr6:2391259-2391260	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs547663010	chr6:2391278-2391279	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs550541124	chr6:2391294-2391295	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs148859151	chr6:2391315-2391316	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs192491269	chr6:2391316-2391317	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs375840653	chr6:2391349-2391350	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs555701219	chr6:2391421-2391422	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs569637148	chr6:2391475-2391476	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs535173574	chr6:2391486-2391487	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs183832038	chr6:2391495-2391496	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs572135744	chr6:2391498-2391499	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs12209220	chr6:2391524-2391525	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs4959654	chr6:2391525-2391526	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs34200997	chr6:2391566-2391567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188488514	chr6:2391602-2391603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142550864	chr6:2391616-2391617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs114233163	chr6:2391629-2391630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191848484	chr6:2391656-2391657	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562238326	chr6:2391663-2391664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184400737	chr6:2391724-2391725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs74847707	chr6:2391760-2391761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113860401	chr6:2391814-2391815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570721470	chr6:2391815-2391816	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533401349	chr6:2391826-2391827	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550084128	chr6:2391873-2391874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs538516835	chr6:2391897-2391898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569517379	chr6:2391905-2391906	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs77238841	chr6:2391917-2391918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555150057	chr6:2391919-2391920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7773388	chr6:2391963-2391964	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs147616657	chr6:2391996-2391997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374518203	chr6:2392000-2392001	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Uveal melanoma	20484589	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD

Chromatin state (count:160 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:2362400-2391800	Weak transcription	Fetal Intestine Small	intestine
2	chr6:2362400-2397200	Weak transcription	Liver	Liver
3	chr6:2362800-2397200	Weak transcription	Left Ventricle	heart
4	chr6:2381000-2397200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:2382800-2397000	Weak transcription	Fetal Stomach	stomach
6	chr6:2383000-2396800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr6:2383000-2397600	Weak transcription	Gastric	stomach
8	chr6:2383200-2391800	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr6:2383200-2398800	Weak transcription	Stomach Smooth Muscle	stomach
10	chr6:2383800-2391600	Weak transcription	Aorta	Aorta
11	chr6:2386200-2391400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr6:2387000-2396800	Weak transcription	Fetal Muscle Leg	muscle
13	chr6:2387600-2398200	Weak transcription	Ovary	ovary
14	chr6:2387800-2397400	Weak transcription	Adipose Nuclei	Adipose
15	chr6:2389400-2397600	Weak transcription	Pancreas	Pancrea
16	chr6:2389600-2396800	Weak transcription	Spleen	Spleen
17	chr6:2389600-2397200	Weak transcription	Lung	lung
18	chr6:2389600-2398600	Weak transcription	Esophagus	oesophagus
19	chr6:2389800-2394200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr6:2390600-2391600	Strong transcription	Primary T cells from cord blood	blood
21	chr6:2390600-2399000	Weak transcription	Fetal Intestine Large	intestine
22	chr6:2391600-2392400	Strong transcription	Aorta	Aorta
23	chr6:2391600-2399400	Weak transcription	Primary T cells from cord blood	blood
24	chr6:2391800-2392400	Strong transcription	Skeletal Muscle Male	skeletal muscle
25	chr6:2391800-2392800	Strong transcription	Fetal Intestine Small	intestine
26	chr6:2392400-2400600	Weak transcription	Aorta	Aorta
27	chr6:2392400-2414400	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr6:2392800-2397600	Weak transcription	Fetal Intestine Small	intestine
29	chr6:2394400-2397600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr6:2395400-2403800	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr6:2396400-2396800	Enhancers	HSMMtube	muscle
32	chr6:2396400-2397200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr6:2396600-2397000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr6:2396600-2397400	Enhancers	HSMM	muscle
35	chr6:2396800-2397000	Enhancers	Brain Cingulate Gyrus	brain
36	chr6:2396800-2397200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr6:2396800-2397200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr6:2396800-2397200	Enhancers	NHDF-Ad	bronchial
39	chr6:2396800-2397200	Enhancers	NHLF	lung
40	chr6:2396800-2397200	Enhancers	Osteobl	bone
41	chr6:2396800-2397400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr6:2396800-2397400	Enhancers	Muscle Satellite Cultured Cells	--
43	chr6:2396800-2397800	Enhancers	Spleen	Spleen
44	chr6:2396800-2397800	Flanking Active TSS	HSMMtube	muscle
45	chr6:2396800-2398000	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr6:2396800-2398000	Enhancers	Fetal Lung	lung
47	chr6:2396800-2398200	Enhancers	Fetal Muscle Leg	muscle
48	chr6:2396800-2400800	Weak transcription	Primary hematopoietic stem cells	blood
49	chr6:2396800-2415400	Weak transcription	Rectal Smooth Muscle	rectum
50	chr6:2397000-2397200	Enhancers	Brain Anterior Caudate	brain

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