Variant report

Variant	nsv1059785
Chromosome Location	chr19:35849061-35861767
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:137)
CpG islands
(count:244)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:137 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:35849261-35849449	K562	blood:	n/a	n/a
2	BACH1	chr19:35851866-35852079	K562	blood:	n/a	n/a
3	CEBPB	chr19:35849017-35849385	IMR90	lung:	n/a	chr19:35849192-35849203
4	CEBPB	chr19:35861294-35861521	HepG2	liver:	n/a	chr19:35861400-35861411
5	CEBPB	chr19:35849027-35849357	HepG2	liver:	n/a	chr19:35849192-35849203
6	CEBPB	chr19:35849029-35849356	A549	lung:	n/a	chr19:35849192-35849203
7	CEBPB	chr19:35849083-35849292	H1-hESC	embryonic stem cell:	n/a	chr19:35849192-35849203
8	CEBPB	chr19:35849039-35849353	Hela-S3	cervix:	n/a	chr19:35849192-35849203
9	CEBPB	chr19:35861266-35861524	A549	lung:	n/a	chr19:35861400-35861411
10	CEBPB	chr19:35849037-35849249	K562	blood:	n/a	chr19:35849192-35849203
11	CEBPB	chr19:35861320-35861547	K562	blood:	n/a	chr19:35861400-35861411
12	CEBPB	chr19:35849025-35849368	K562	blood:	n/a	chr19:35849192-35849203
13	CEBPB	chr19:35861291-35861545	IMR90	lung:	n/a	chr19:35861400-35861411
14	CTCF	chr19:35850172-35850235	GM12891	blood:	n/a	n/a
15	CTCF	chr19:35849820-35849970	GM12864	blood:	n/a	n/a
16	CTCF	chr19:35849861-35850024	ProgFib	skin:	n/a	n/a
17	CTCF	chr19:35849814-35849997	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr19:35849820-35849970	A549	lung:	n/a	n/a
19	CTCF	chr19:35851457-35851512	GM12891	blood:	n/a	n/a
20	CTCF	chr19:35849780-35849930	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr19:35849868-35850029	A549	lung:	n/a	n/a
22	CTCF	chr19:35849796-35850090	GM12891	blood:	n/a	n/a
23	CTCF	chr19:35849790-35850033	K562	blood:	n/a	n/a
24	CTCF	chr19:35849840-35849990	HCM	heart:	n/a	n/a
25	CTCF	chr19:35849819-35849993	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr19:35849760-35849910	GM12874	blood:	n/a	n/a
27	CTCF	chr19:35849894-35849995	MCF-7	breast:	n/a	n/a
28	CTCF	chr19:35849857-35850020	GM10248	blood:	n/a	n/a
29	CTCF	chr19:35849780-35849930	GM12874	blood:	n/a	n/a
30	CTCF	chr19:35849820-35849970	GM12868	blood:	n/a	n/a
31	CTCF	chr19:35849824-35850062	K562	blood:	n/a	n/a
32	CTCF	chr19:35849820-35849970	GM12866	blood:	n/a	n/a
33	CTCF	chr19:35849830-35850062	GM12892	blood:	n/a	n/a
34	CTCF	chr19:35849864-35850076	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr19:35849884-35850011	GM13976	blood:	n/a	n/a
36	CTCF	chr19:35849817-35850032	GM20000	blood:	n/a	n/a
37	CTCF	chr19:35849891-35850044	NHEK	skin:	n/a	n/a
38	CTCF	chr19:35849676-35850178	K562	blood:	n/a	n/a
39	CTCF	chr19:35849874-35849999	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr19:35849840-35849990	GM12869	blood:	n/a	n/a
41	CTCF	chr19:35849869-35850041	GM10266	blood:	n/a	n/a
42	CTCF	chr19:35849858-35849961	HepG2	liver:	n/a	n/a
43	CTCF	chr19:35849840-35849990	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr19:35849780-35849930	AG04449	skin:	n/a	n/a
45	CTCF	chr19:35849862-35850049	Fibrobl	skin:	n/a	n/a
46	CTCF	chr19:35849856-35850054	Gliobla	brain:	n/a	n/a
47	CTCF	chr19:35849780-35849930	GM12873	blood:	n/a	n/a
48	CTCF	chr19:35849798-35850068	GM13977	blood:	n/a	n/a
49	CTCF	chr19:35849830-35850072	GM19240	blood:	n/a	n/a
50	CTCF	chr19:35849840-35849990	GM12866	blood:	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	chr19:35850463-35850513	GM06990	blood:	n/a
2	chr19:35849176-35849226	Caco-2	colon:	n/a
3	chr19:35849393-35849443	LNCaP	prostate:	n/a
4	chr19:35849393-35849443	SK-N-SH_RA	brain:	n/a
5	chr19:35849393-35849443	PFSK-1	brain:	n/a
6	chr19:35849024-35849074	HUVEC	blood vessel:	n/a
7	chr19:35849024-35849074	AG10803	skin:	n/a
8	chr19:35849176-35849226	HAEpiC	amniotic membrane:	n/a
9	chr19:35849024-35849074	MCF-7	breast:	n/a
10	chr19:35849393-35849443	Jurkat	blood:	n/a
11	chr19:35849176-35849226	MCF-7	breast:	n/a
12	chr19:35850463-35850513	SK-N-MC	brain:	n/a
13	chr19:35849024-35849074	SK-N-MC	brain:	n/a
14	chr19:35849176-35849226	NH-A	brain:	n/a
15	chr19:35850463-35850513	U87	brain:	n/a
16	chr19:35849393-35849443	Hepatocyte	liver:	n/a
17	chr19:35849024-35849074	Hela-S3	cervix:	n/a
18	chr19:35849176-35849226	BJ	skin:	n/a
19	chr19:35849176-35849226	LNCaP	prostate:	n/a
20	chr19:35849393-35849443	BE2_C	brain:	n/a
21	chr19:35850463-35850513	NT2-D1	testis:	n/a
22	chr19:35849176-35849226	HRE	kidney:	n/a
23	chr19:35849176-35849226	HMEC	breast:	n/a
24	chr19:35849176-35849226	ProgFib	skin:	n/a
25	chr19:35849024-35849074	HRPEpiC	eye:	n/a
26	chr19:35849393-35849443	SK-N-MC	brain:	n/a
27	chr19:35849393-35849443	PANC-1	pancreas:	n/a
28	chr19:35849024-35849074	RPTEC	kidney:	n/a
29	chr19:35849176-35849226	U87	brain:	n/a
30	chr19:35849393-35849443	GM06990	blood:	n/a
31	chr19:35849393-35849443	AoSMC	blood vessel:	n/a
32	chr19:35849393-35849443	HepG2	liver:	n/a
33	chr19:35849393-35849443	H1-hESC	embryonic stem cell:	embryo
34	chr19:35849393-35849443	HRPEpiC	eye:	n/a
35	chr19:35849176-35849226	SK-N-SH	brain:	n/a
36	chr19:35850463-35850513	IMR90	lung:	fetal
37	chr19:35849393-35849443	HUVEC	blood vessel:	n/a
38	chr19:35849393-35849443	HAEpiC	amniotic membrane:	n/a
39	chr19:35850463-35850513	ECC-1	luminal epithelium:	n/a
40	chr19:35850463-35850513	AG09309	skin:	n/a
41	chr19:35850463-35850513	H1-hESC	embryonic stem cell:	embryo
42	chr19:35850463-35850513	HAEpiC	amniotic membrane:	n/a
43	chr19:35849024-35849074	GM12878	blood:	n/a
44	chr19:35849393-35849443	AG04449	skin:	fetal
45	chr19:35849393-35849443	HMEC	breast:	n/a
46	chr19:35850463-35850513	HNPCEpiC	eye:	n/a
47	chr19:35850463-35850513	SK-N-SH	brain:	n/a
48	chr19:35850463-35850513	HRPEpiC	eye:	n/a
49	chr19:35849393-35849443	NHDF-neo	bronchial:	n/a
50	chr19:35849024-35849074	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:35847716..35849933-chr19:35855045..35856568,2	MCF-7	breast:

No data

Variant related genes	Relation type
FFAR3	TF binding region
GPR42	TF binding region
FFAR3	CpG island
GPR42	CpG island
ENSG00000185897	chromatin interactions

Extended variants
information (count: 365 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:365 , 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	rs17272288	chr19:35849061-35849062	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs367544251	chr19:35849136-35849137	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs537004693	chr19:35849143-35849144	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs537890763	chr19:35849176-35849177	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs143244108	chr19:35849183-35849184	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs58199607	chr19:35849184-35849185	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs536178273	chr19:35849273-35849274	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs146704794	chr19:35849283-35849284	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs555975639	chr19:35849306-35849307	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs572634896	chr19:35849343-35849344	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs381099	chr19:35849410-35849411	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs375854528	chr19:35849428-35849429	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs369874702	chr19:35849436-35849437	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs558280055	chr19:35849441-35849442	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs10412120	chr19:35849447-35849448	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs539350244	chr19:35849471-35849472	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs543374650	chr19:35849472-35849473	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs59198030	chr19:35849563-35849564	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs62109580	chr19:35849666-35849667	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs369303830	chr19:35849690-35849691	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs573573596	chr19:35849691-35849692	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs542544927	chr19:35849738-35849739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368520877	chr19:35849742-35849743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528333217	chr19:35849755-35849756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs146397125	chr19:35849813-35849814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551288253	chr19:35849824-35849825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs368567016	chr19:35849841-35849842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371169601	chr19:35849849-35849850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530535002	chr19:35849856-35849857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs150256974	chr19:35849883-35849884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs550566313	chr19:35849897-35849898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148149328	chr19:35849909-35849910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs62109581	chr19:35849926-35849927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375665593	chr19:35849930-35849931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs202228986	chr19:35849931-35849932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs138919331	chr19:35849933-35849934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs139872810	chr19:35849937-35849938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs368240354	chr19:35849938-35849939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs141595495	chr19:35849939-35849940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs200224629	chr19:35849940-35849941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs566139658	chr19:35849942-35849943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372231935	chr19:35849945-35849946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs367794314	chr19:35849946-35849947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs578021833	chr19:35849960-35849961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs146184076	chr19:35849966-35849967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs139036566	chr19:35849973-35849974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs556917621	chr19:35850006-35850007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs202122950	chr19:35850007-35850008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149009291	chr19:35850022-35850023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371280742	chr19:35850076-35850077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Gastric cancer	21811585	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35838200-35849200	Weak transcription	Brain Hippocampus Middle	brain
2	chr19:35847200-35852000	Weak transcription	GM12878-XiMat	blood
3	chr19:35848200-35849200	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr19:35848200-35849400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
5	chr19:35848200-35849600	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr19:35848400-35849400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr19:35848400-35849400	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr19:35848400-35849400	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr19:35848400-35849400	Enhancers	Fetal Muscle Leg	muscle
10	chr19:35848400-35849400	Enhancers	HepG2	liver
11	chr19:35848400-35849600	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr19:35848400-35849600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr19:35848400-35849600	Enhancers	Placenta	Placenta
14	chr19:35848600-35849200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr19:35848600-35849400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr19:35848600-35849400	Enhancers	Gastric	stomach
17	chr19:35848600-35849400	Enhancers	Pancreas	Pancrea
18	chr19:35848800-35849200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr19:35848800-35849200	Enhancers	Fetal Brain Female	brain
20	chr19:35848800-35849200	Enhancers	Fetal Muscle Trunk	muscle
21	chr19:35848800-35849200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
22	chr19:35848800-35849200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
23	chr19:35848800-35849400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr19:35848800-35849400	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr19:35848800-35849400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr19:35848800-35849400	Flanking Active TSS	Adipose Nuclei	Adipose
27	chr19:35848800-35849400	Enhancers	Liver	Liver
28	chr19:35848800-35849400	Enhancers	Brain Germinal Matrix	brain
29	chr19:35848800-35849400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
30	chr19:35848800-35849400	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr19:35848800-35849600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
32	chr19:35848800-35849600	Enhancers	Primary hematopoietic stem cells	blood
33	chr19:35848800-35849600	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr19:35848800-35849600	Enhancers	Lung	lung
35	chr19:35849000-35849200	Enhancers	Fetal Intestine Small	intestine
36	chr19:35849000-35849200	Bivalent Enhancer	K562	blood
37	chr19:35849000-35849400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr19:35849000-35849400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr19:35849000-35849400	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr19:35849000-35849400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr19:35849000-35849400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
42	chr19:35849000-35849400	Flanking Active TSS	Fetal Lung	lung
43	chr19:35849000-35849400	Enhancers	Ovary	ovary
44	chr19:35849000-35849400	Enhancers	Spleen	Spleen
45	chr19:35849200-35849400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
46	chr19:35849200-35849400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
47	chr19:35849200-35849400	Enhancers	Brain Hippocampus Middle	brain
48	chr19:35849200-35849400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
49	chr19:35849200-35849600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
50	chr19:35849200-35849600	Enhancers	Stomach Mucosa	stomach

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