Variant report

Variant	nsv601146
Chromosome Location	chr6:24166233-24215665
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:296)
CpG islands
(count:244)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:24205162-24205688	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:24205240-24205558	K562	blood:	n/a	n/a
3	ARID3A	chr6:24198151-24198535	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:24195303-24195911	HepG2	liver:	n/a	n/a
5	CEBPB	chr6:24215023-24215330	MCF-7	breast:	n/a	chr6:24215148-24215161 chr6:24215149-24215160 chr6:24215148-24215161 chr6:24215148-24215159
6	CEBPB	chr6:24215037-24215293	HepG2	liver:	n/a	chr6:24215148-24215161 chr6:24215149-24215160 chr6:24215148-24215161 chr6:24215148-24215159
7	CEBPB	chr6:24195569-24195900	HepG2	liver:	n/a	n/a
8	CEBPB	chr6:24205204-24205424	HepG2	liver:	n/a	n/a
9	CEBPB	chr6:24208619-24208741	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr6:24183379-24183579	HepG2	liver:	n/a	n/a
11	CEBPB	chr6:24195246-24195931	HepG2	liver:	n/a	n/a
12	CEBPD	chr6:24195620-24195925	HepG2	liver:	n/a	n/a
13	CTCF	chr6:24201304-24201347	LNCaP	prostate:	n/a	n/a
14	CTCF	chr6:24205280-24205430	HCM	heart:	n/a	n/a
15	CTCF	chr6:24205222-24205428	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr6:24205300-24205450	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr6:24205139-24205638	MCF-7	breast:	n/a	n/a
18	CTCF	chr6:24205180-24205330	A549	lung:	n/a	n/a
19	CTCF	chr6:24205145-24205607	GM12878	blood:	n/a	n/a
20	CTCF	chr6:24205300-24205450	HVMF	connective:	n/a	n/a
21	CTCF	chr6:24205300-24205450	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr6:24205300-24205450	AG04449	skin:	n/a	n/a
23	CTCF	chr6:24205192-24205658	MCF-7	breast:	n/a	n/a
24	CTCF	chr6:24205300-24205450	HUVEC	blood vessel:	n/a	n/a
25	CTCF	chr6:24205218-24205558	ECC-1	luminal epithelium:	n/a	n/a
26	CTCF	chr6:24205278-24205499	A549	lung:	n/a	n/a
27	CTCF	chr6:24203362-24203396	GM13977	blood:	n/a	n/a
28	CTCF	chr6:24205616-24205707	K562	blood:	n/a	n/a
29	CTCF	chr6:24205178-24205544	HepG2	liver:	n/a	n/a
30	CTCF	chr6:24205280-24205430	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr6:24205280-24205430	GM12864	blood:	n/a	n/a
32	CTCF	chr6:24205034-24205663	SK-N-SH	brain:	n/a	n/a
33	CTCF	chr6:24205320-24205470	GM12878	blood:	n/a	n/a
34	CTCF	chr6:24205280-24205430	RPTEC	kidney:	n/a	n/a
35	CTCF	chr6:24205300-24205450	AG09319	gingival:	n/a	n/a
36	CTCF	chr6:24205280-24205430	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr6:24205277-24205420	Fibrobl	skin:	n/a	n/a
38	CTCF	chr6:24205480-24205630	NHEK	skin:	n/a	n/a
39	CTCF	chr6:24205320-24205470	AG09309	skin:	n/a	n/a
40	CTCF	chr6:24205400-24205550	WI-38	lung:	n/a	n/a
41	CTCF	chr6:24205195-24205432	A549	lung:	n/a	n/a
42	CTCF	chr6:24205320-24205470	HCT-116	colon:	n/a	n/a
43	CTCF	chr6:24205240-24205390	NHEK	skin:	n/a	n/a
44	CTCF	chr6:24205100-24205250	HAc	cerebellar:	n/a	n/a
45	CTCF	chr6:24205320-24205470	HMEC	breast:	n/a	n/a
46	CTCF	chr6:24205184-24205500	HepG2	liver:	n/a	n/a
47	CTCF	chr6:24205300-24205450	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr6:24205255-24205504	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr6:24205300-24205450	GM12864	blood:	n/a	n/a
50	CTCF	chr6:24205243-24205504	Gliobla	brain:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:24205566-24205616	AG04449	skin:	fetal
2	chr6:24206177-24206227	T-47D	breast:	n/a
3	chr6:24205566-24205616	Hela-S3	cervix:	n/a
4	chr6:24206886-24206936	HAEpiC	amniotic membrane:	n/a
5	chr6:24206886-24206936	Jurkat	blood:	n/a
6	chr6:24205566-24205616	MCF10A-Er-Src	breast:	n/a
7	chr6:24206886-24206936	IMR90	lung:	fetal
8	chr6:24205566-24205616	HRE	kidney:	n/a
9	chr6:24205566-24205616	Jurkat	blood:	n/a
10	chr6:24205566-24205616	HRPEpiC	eye:	n/a
11	chr6:24172312-24172362	HEEpiC	esophagus:	n/a
12	chr6:24205566-24205616	NH-A	brain:	n/a
13	chr6:24206886-24206936	GM19239	blood:	n/a
14	chr6:24172312-24172362	BJ	skin:	n/a
15	chr6:24206177-24206227	AG04449	skin:	fetal
16	chr6:24172312-24172362	NT2-D1	testis:	n/a
17	chr6:24206177-24206227	HIPEpiC	eye:	n/a
18	chr6:24206177-24206227	HRE	kidney:	n/a
19	chr6:24206886-24206936	HRE	kidney:	n/a
20	chr6:24205566-24205616	HL-60	blood:	n/a
21	chr6:24206177-24206227	PFSK-1	brain:	n/a
22	chr6:24205566-24205616	HCF	heart:	n/a
23	chr6:24206177-24206227	LNCaP	prostate:	n/a
24	chr6:24206177-24206227	SKMC	muscle:	n/a
25	chr6:24172312-24172362	AoSMC	blood vessel:	n/a
26	chr6:24206886-24206936	HCT-116	colon:	n/a
27	chr6:24172312-24172362	SK-N-SH	brain:	n/a
28	chr6:24172312-24172362	NHBE	bronchial:	n/a
29	chr6:24206177-24206227	NHBE	bronchial:	n/a
30	chr6:24206886-24206936	LNCaP	prostate:	n/a
31	chr6:24172312-24172362	HMEC	breast:	n/a
32	chr6:24172312-24172362	CMK	blood:	n/a
33	chr6:24205566-24205616	GM19239	blood:	n/a
34	chr6:24206177-24206227	CMK	blood:	n/a
35	chr6:24206177-24206227	BJ	skin:	n/a
36	chr6:24205566-24205616	NHBE	bronchial:	n/a
37	chr6:24172312-24172362	LNCaP	prostate:	n/a
38	chr6:24206886-24206936	SK-N-SH	brain:	n/a
39	chr6:24172312-24172362	SAEC	small airway:	n/a
40	chr6:24172312-24172362	GM19239	blood:	n/a
41	chr6:24205566-24205616	A549	lung:	n/a
42	chr6:24206177-24206227	ProgFib	skin:	n/a
43	chr6:24172312-24172362	ProgFib	skin:	n/a
44	chr6:24206886-24206936	GM12878	blood:	n/a
45	chr6:24206886-24206936	Hepatocyte	liver:	n/a
46	chr6:24205566-24205616	GM12891	blood:	n/a
47	chr6:24206177-24206227	HL-60	blood:	n/a
48	chr6:24206177-24206227	PrEC	prostate:	n/a
49	chr6:24205566-24205616	HMEC	breast:	n/a
50	chr6:24172312-24172362	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr6:24211897..24214693-chr6:24215631..24218081,2	MCF-7	breast:
2	chr6:24211897..24214693-chr6:24215631..24218081,2	MCF-7	breast:
3	chr15:65596739..65598774-chr6:24167185..24169291,2	K562	blood:

No data

Variant related genes	Relation type
DCDC2	TF binding region
ENSG00000251830	TF binding region
DCDC2	CpG island
ENSG00000251830	CpG island
ENSG00000200156	chromatin interactions

Extended variants
information (count: 2202 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2202 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11751907	chr6:24166233-24166234	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs545129818	chr6:24166260-24166261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564890236	chr6:24166289-24166290	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs530622829	chr6:24166345-24166346	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs550425771	chr6:24166352-24166353	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs567207708	chr6:24166374-24166375	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs529964338	chr6:24166393-24166394	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs558941064	chr6:24166447-24166448	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs538215815	chr6:24166470-24166471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556601416	chr6:24166471-24166472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35671434	chr6:24166540-24166541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs397776314	chr6:24166541-24166542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546111075	chr6:24166570-24166571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs16888745	chr6:24166593-24166594	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs386698067	chr6:24166640-24166641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs9467059	chr6:24166642-24166643	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs569449517	chr6:24166657-24166658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554665206	chr6:24166687-24166688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs150292567	chr6:24166747-24166748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192959387	chr6:24166769-24166770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs137947384	chr6:24166858-24166859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs182878448	chr6:24166865-24166866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140713797	chr6:24166873-24166874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187792215	chr6:24166938-24166939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35935249	chr6:24167003-24167004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544731609	chr6:24167021-24167022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565007476	chr6:24167033-24167034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192305311	chr6:24167078-24167079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530553747	chr6:24167090-24167091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543980842	chr6:24167129-24167130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34803284	chr6:24167130-24167131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575882329	chr6:24167131-24167132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112792246	chr6:24167133-24167134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543763149	chr6:24167198-24167199	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs73391913	chr6:24167242-24167243	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs562133007	chr6:24167271-24167272	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs115062864	chr6:24167303-24167304	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs532808432	chr6:24167310-24167311	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs576323052	chr6:24167386-24167387	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs56974062	chr6:24167478-24167479	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs532557692	chr6:24167602-24167603	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs551765069	chr6:24167638-24167639	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs531218591	chr6:24167667-24167668	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs9467060	chr6:24167673-24167674	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs569360751	chr6:24167707-24167708	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs183689860	chr6:24167712-24167713	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs9393533	chr6:24167748-24167749	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs568711923	chr6:24167750-24167751	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs373574504	chr6:24167791-24167792	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs4582376	chr6:24167807-24167808	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:101)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	16790693	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Williams-beuren syndrome	16971481	CNVD
Uveal melanoma	20484589	CNVD

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24153800-24200800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:24163600-24177600	Weak transcription	Fetal Kidney	kidney
3	chr6:24164400-24183800	Weak transcription	Pancreas	Pancrea
4	chr6:24170000-24171600	Weak transcription	HepG2	liver
5	chr6:24171600-24173200	Strong transcription	HepG2	liver
6	chr6:24171600-24182800	Weak transcription	Fetal Intestine Small	intestine
7	chr6:24172800-24194800	Weak transcription	Fetal Intestine Large	intestine
8	chr6:24173200-24174000	Weak transcription	HepG2	liver
9	chr6:24174000-24179600	Strong transcription	HepG2	liver
10	chr6:24177600-24179600	Strong transcription	Fetal Kidney	kidney
11	chr6:24177800-24198400	Weak transcription	A549	lung
12	chr6:24179600-24181400	Weak transcription	Fetal Kidney	kidney
13	chr6:24179600-24181400	Weak transcription	HepG2	liver
14	chr6:24181400-24184000	Strong transcription	Fetal Kidney	kidney
15	chr6:24181400-24189600	Strong transcription	HepG2	liver
16	chr6:24182800-24184600	ZNF genes & repeats	Fetal Intestine Small	intestine
17	chr6:24183800-24184200	ZNF genes & repeats	Pancreas	Pancrea
18	chr6:24184000-24184200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:24184000-24184200	ZNF genes & repeats	Fetal Kidney	kidney
20	chr6:24184200-24185800	Weak transcription	Fetal Kidney	kidney
21	chr6:24184200-24195200	Weak transcription	Pancreas	Pancrea
22	chr6:24184600-24195000	Weak transcription	Fetal Intestine Small	intestine
23	chr6:24185800-24186600	Strong transcription	Fetal Kidney	kidney
24	chr6:24186400-24187000	Enhancers	Fetal Brain Male	brain
25	chr6:24186600-24196000	Weak transcription	Fetal Kidney	kidney
26	chr6:24187000-24189400	Weak transcription	Fetal Brain Male	brain
27	chr6:24189000-24189200	Enhancers	Fetal Brain Female	brain
28	chr6:24189400-24190000	Enhancers	Fetal Brain Male	brain
29	chr6:24189600-24190800	Weak transcription	HepG2	liver
30	chr6:24189800-24190000	Enhancers	Fetal Brain Female	brain
31	chr6:24190800-24191200	Strong transcription	HepG2	liver
32	chr6:24191200-24193200	Weak transcription	HepG2	liver
33	chr6:24192000-24192200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr6:24193200-24194800	Enhancers	HepG2	liver
35	chr6:24194800-24197000	Enhancers	Fetal Intestine Large	intestine
36	chr6:24194800-24199400	Genic enhancers	HepG2	liver
37	chr6:24195000-24195200	Enhancers	Fetal Intestine Small	intestine
38	chr6:24195000-24196200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:24195000-24196200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr6:24195200-24195400	Genic enhancers	Pancreas	Pancrea
41	chr6:24195200-24195600	Weak transcription	Fetal Intestine Small	intestine
42	chr6:24195200-24196000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:24195200-24196000	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr6:24195400-24196000	Enhancers	Pancreas	Pancrea
45	chr6:24195600-24196400	Enhancers	Fetal Intestine Small	intestine
46	chr6:24195800-24197000	Enhancers	Stomach Mucosa	stomach
47	chr6:24196000-24196600	Weak transcription	Pancreas	Pancrea
48	chr6:24196000-24197400	Strong transcription	Fetal Kidney	kidney
49	chr6:24196400-24205400	Weak transcription	Fetal Intestine Small	intestine
50	chr6:24196600-24196800	Enhancers	Pancreas	Pancrea

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links