Variant report

Variant	esv11554
Chromosome Location	chr22:30280400-30298271
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:36)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:36 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr22:30291559-30291624	HepG2	liver:	n/a	chr22:30291581-30291592
2	CEBPB	chr22:30297362-30297676	K562	blood:	n/a	n/a
3	CEBPB	chr22:30297366-30297631	K562	blood:	n/a	n/a
4	CEBPB	chr22:30282643-30282930	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr22:30297405-30297626	K562	blood:	n/a	n/a
6	CEBPB	chr22:30282656-30282856	HepG2	liver:	n/a	n/a
7	CEBPB	chr22:30291550-30291641	K562	blood:	n/a	chr22:30291581-30291592
8	CTCF	chr22:30281784-30281810	LNCaP	prostate:	n/a	n/a
9	CTCF	chr22:30281772-30281782	LNCaP	prostate:	n/a	n/a
10	CTCF	chr22:30280901-30280978	Lung_OC	lung:	n/a	n/a
11	CUX1	chr22:30296240-30296363	GM12878	blood:	n/a	n/a
12	CUX1	chr22:30295405-30295569	K562	blood:	n/a	chr22:30295529-30295543 chr22:30295502-30295511
13	FOS	chr22:30282701-30282953	MCF10A-Er-Src	breast:	n/a	n/a
14	FOXA2	chr22:30293592-30293826	A549	lung:	n/a	n/a
15	GATA3	chr22:30283718-30284123	SH-SY5Y	brain:	n/a	n/a
16	HEY1	chr22:30280902-30281166	K562	blood:	n/a	n/a
17	JUND	chr22:30297520-30297671	K562	blood:	n/a	n/a
18	MAFK	chr22:30295919-30295995	IMR90	lung:	n/a	chr22:30295942-30295953 chr22:30295941-30295952
19	MAFK	chr22:30295778-30296107	HepG2	liver:	n/a	chr22:30295942-30295953 chr22:30295941-30295952
20	MAX	chr22:30282695-30282838	NB4	blood:	n/a	n/a
21	MAX	chr22:30297426-30297673	NB4	blood:	n/a	chr22:30297502-30297512
22	MXI1	chr22:30278703-30280515	SK-N-SH	brain:	n/a	chr22:30279039-30279048
23	MYC	chr22:30297281-30297416	MCF10A-Er-Src	breast:	n/a	n/a
24	MYC	chr22:30282615-30283015	MCF10A-Er-Src	breast:	n/a	n/a
25	MYC	chr22:30282679-30282874	NB4	blood:	n/a	n/a
26	MYC	chr22:30297476-30297654	K562	blood:	n/a	chr22:30297502-30297512
27	MYC	chr22:30294696-30294733	GM12878	blood:	n/a	n/a
28	POLR2A	chr22:30282010-30282107	MCF10A-Er-Src	breast:	n/a	n/a
29	SPI1	chr22:30297307-30297806	HL-60	blood:	n/a	n/a
30	STAT3	chr22:30282692-30282942	MCF10A-Er-Src	breast:	n/a	chr22:30282874-30282882
31	STAT3	chr22:30283405-30283605	MCF10A-Er-Src	breast:	n/a	n/a
32	STAT3	chr22:30282679-30282988	MCF10A-Er-Src	breast:	n/a	chr22:30282874-30282882
33	TCF7L2	chr22:30288420-30289029	HEK293	kidney:	n/a	chr22:30288573-30288587 chr22:30288572-30288588
34	ZNF384	chr22:30285235-30285348	K562	blood:	n/a	n/a
35	ZNF384	chr22:30280593-30280596	GM12878	blood:	n/a	n/a
36	ZNF384	chr22:30280497-30280530	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:30283578-30283628	U87	brain:	n/a
2	chr22:30283578-30283628	K562	blood:	n/a
3	chr22:30283578-30283628	HAEpiC	amniotic membrane:	n/a
4	chr22:30283578-30283628	H1-hESC	embryonic stem cell:	embryo
5	chr22:30283578-30283628	SK-N-SH	brain:	n/a
6	chr22:30283578-30283628	ProgFib	skin:	n/a
7	chr22:30283578-30283628	HRPEpiC	eye:	n/a
8	chr22:30283578-30283628	HRCEpiC	kidney:	n/a
9	chr22:30283578-30283628	HL-60	blood:	n/a
10	chr22:30283578-30283628	PANC-1	pancreas:	n/a
11	chr22:30283578-30283628	HPAEpiC	pulmonary alveolar:	n/a
12	chr22:30283578-30283628	AoSMC	blood vessel:	n/a
13	chr22:30283578-30283628	PrEC	prostate:	n/a
14	chr22:30283578-30283628	HIPEpiC	eye:	n/a
15	chr22:30283578-30283628	AG09319	gingival:	n/a
16	chr22:30283578-30283628	NHBE	bronchial:	n/a
17	chr22:30283578-30283628	HRE	kidney:	n/a
18	chr22:30283578-30283628	RPTEC	kidney:	n/a
19	chr22:30283578-30283628	NH-A	brain:	n/a
20	chr22:30283578-30283628	BJ	skin:	n/a
21	chr22:30283578-30283628	NT2-D1	testis:	n/a
22	chr22:30283578-30283628	AG04450	lung:	fetal
23	chr22:30283578-30283628	Caco-2	colon:	n/a
24	chr22:30283578-30283628	NHDF-neo	bronchial:	n/a
25	chr22:30283578-30283628	GM19239	blood:	n/a
26	chr22:30283578-30283628	GM12891	blood:	n/a
27	chr22:30283578-30283628	Hepatocyte	liver:	n/a
28	chr22:30283578-30283628	MCF-7	breast:	n/a
29	chr22:30283578-30283628	HMEC	breast:	n/a
30	chr22:30283578-30283628	HCPEpiC	choroid plexus:	n/a
31	chr22:30283578-30283628	SAEC	small airway:	n/a
32	chr22:30283578-30283628	NB4	blood:	n/a
33	chr22:30283578-30283628	Jurkat	blood:	n/a
34	chr22:30283578-30283628	CMK	blood:	n/a
35	chr22:30283578-30283628	Hela-S3	cervix:	n/a
36	chr22:30283578-30283628	HNPCEpiC	eye:	n/a
37	chr22:30283578-30283628	A549	lung:	n/a
38	chr22:30283578-30283628	ECC-1	luminal epithelium:	n/a
39	chr22:30283578-30283628	MCF10A-Er-Src	breast:	n/a
40	chr22:30283578-30283628	AG04449	skin:	fetal
41	chr22:30283578-30283628	GM06990	blood:	n/a
42	chr22:30283578-30283628	HepG2	liver:	n/a
43	chr22:30283578-30283628	HUVEC	blood vessel:	n/a
44	chr22:30283578-30283628	HCF	heart:	n/a
45	chr22:30283578-30283628	HCM	heart:	n/a
46	chr22:30283578-30283628	PFSK-1	brain:	n/a
47	chr22:30283578-30283628	HEK293	kidney:	embryo
48	chr22:30283578-30283628	SKMC	muscle:	n/a
49	chr22:30283578-30283628	IMR90	lung:	fetal
50	chr22:30283578-30283628	AG09309	skin:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:30289517..30291568-chr22:30301427..30303381,2	K562	blood:
2	chr22:30280125..30281940-chr22:30289079..30291294,2	MCF-7	breast:
3	chr22:30280125..30281940-chr22:30289079..30291294,2	MCF-7	breast:
4	chr22:30208243..30210090-chr22:30279066..30280884,2	MCF-7	breast:
5	chr22:30288615..30290652-chr22:30302494..30304851,2	MCF-7	breast:
6	chr22:30229506..30231085-chr22:30279535..30281040,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNU6-331P	TF binding region
RNU6-331P	CpG island
ENSG00000100325	chromatin interactions

Extended variants
information (count: 696 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:696 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544839963	chr22:30280439-30280440	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs12628395	chr22:30280450-30280451	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs202147613	chr22:30280513-30280514	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs35960936	chr22:30280541-30280542	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs79426564	chr22:30280563-30280564	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs76224095	chr22:30280564-30280565	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs111444479	chr22:30280569-30280570	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs553021053	chr22:30280615-30280616	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs574879066	chr22:30280626-30280627	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs11704321	chr22:30280637-30280638	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs557365829	chr22:30280656-30280657	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs575427932	chr22:30280678-30280679	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs568681293	chr22:30280743-30280744	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs546114363	chr22:30280797-30280798	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs10222284	chr22:30280801-30280802	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs192136924	chr22:30280811-30280812	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs77162742	chr22:30280900-30280901	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs183055173	chr22:30280911-30280912	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs375308973	chr22:30280924-30280925	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs369674610	chr22:30280958-30280959	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs540434340	chr22:30280961-30280962	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs371920950	chr22:30280973-30280974	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs561729268	chr22:30280990-30280991	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs376572779	chr22:30281024-30281025	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs116535002	chr22:30281038-30281039	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs374706008	chr22:30281057-30281058	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs145969090	chr22:30281098-30281099	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs5763573	chr22:30281099-30281100	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs550305832	chr22:30281103-30281104	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs76229752	chr22:30281118-30281119	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs527854976	chr22:30281130-30281131	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs71398435	chr22:30281131-30281132	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs75037329	chr22:30281138-30281139	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs78078124	chr22:30281150-30281151	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs74701278	chr22:30281162-30281163	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs75932005	chr22:30281163-30281164	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs80016756	chr22:30281187-30281188	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs74945300	chr22:30281195-30281196	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs386820607	chr22:30281199-30281200	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs79671613	chr22:30281200-30281201	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs562529293	chr22:30281215-30281216	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs77856340	chr22:30281216-30281217	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs80129847	chr22:30281220-30281221	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs79566559	chr22:30281226-30281227	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs187023326	chr22:30281270-30281271	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs73161096	chr22:30281277-30281278	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs75539148	chr22:30281292-30281293	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs74765332	chr22:30281297-30281298	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs370473821	chr22:30281318-30281319	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs76452198	chr22:30281320-30281321	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD
Melanoma	17363583	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:687 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30278600-30280400	Active TSS	Fetal Kidney	kidney
2	chr22:30278600-30280600	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr22:30278600-30280600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr22:30278600-30280600	Active TSS	Fetal Brain Female	brain
5	chr22:30278600-30281400	Active TSS	Rectal Mucosa Donor 29	rectum
6	chr22:30278800-30280400	Active TSS	H1 Cell Line	embryonic stem cell
7	chr22:30278800-30280400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr22:30278800-30280400	Active TSS	iPS-20b Cell Line	embryonic stem cell
9	chr22:30278800-30280400	Active TSS	Brain Angular Gyrus	brain
10	chr22:30278800-30280400	Active TSS	Brain Hippocampus Middle	brain
11	chr22:30278800-30280400	Active TSS	Fetal Intestine Large	intestine
12	chr22:30278800-30280400	Active TSS	Fetal Stomach	stomach
13	chr22:30278800-30280400	Active TSS	Fetal Thymus	thymus
14	chr22:30278800-30280400	Active TSS	Ovary	ovary
15	chr22:30278800-30280400	Active TSS	Thymus	Thymus
16	chr22:30278800-30280400	Active TSS	A549	lung
17	chr22:30278800-30280400	Active TSS	K562	blood
18	chr22:30278800-30280600	Active TSS	HUES64 Cell Line	embryonic stem cell
19	chr22:30278800-30280600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr22:30278800-30280600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr22:30278800-30280600	Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr22:30278800-30280600	Active TSS	Brain Inferior Temporal Lobe	brain
23	chr22:30278800-30280600	Active TSS	Brain Substantia Nigra	brain
24	chr22:30278800-30280600	Active TSS	Pancreatic Islets	Pancreatic Islet
25	chr22:30278800-30280600	Active TSS	Fetal Muscle Trunk	muscle
26	chr22:30278800-30280600	Active TSS	Psoas Muscle	Psoas
27	chr22:30278800-30280600	Active TSS	Right Atrium	heart
28	chr22:30278800-30280600	Active TSS	Hela-S3	cervix
29	chr22:30278800-30280600	Active TSS	NHLF	lung
30	chr22:30278800-30280600	Active TSS	Osteobl	bone
31	chr22:30278800-30280800	Active TSS	Skeletal Muscle Female	skeletal muscle
32	chr22:30278800-30280800	Active TSS	HepG2	liver
33	chr22:30278800-30280800	Active TSS	HMEC	breast
34	chr22:30278800-30280800	Active TSS	HSMM	muscle
35	chr22:30278800-30281000	Active TSS	HUES48 Cell Line	embryonic stem cell
36	chr22:30278800-30281200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr22:30278800-30281200	Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr22:30278800-30281200	Active TSS	Stomach Smooth Muscle	stomach
39	chr22:30278800-30282200	Active TSS	GM12878-XiMat	blood
40	chr22:30279000-30280400	Active TSS	iPS-15b Cell Line	embryonic stem cell
41	chr22:30279000-30280400	Active TSS	Primary T cells fromperipheralblood	blood
42	chr22:30279000-30280400	Active TSS	Cortex derived primary cultured neurospheres	brain
43	chr22:30279000-30280400	Active TSS	Fetal Muscle Leg	muscle
44	chr22:30279000-30280600	Active TSS	Colonic Mucosa	Colon
45	chr22:30279000-30280600	Active TSS	Duodenum Mucosa	Duodenum
46	chr22:30279000-30280800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr22:30279000-30280800	Active TSS	Right Ventricle	heart
48	chr22:30279000-30280800	Active TSS	Skeletal Muscle Male	skeletal muscle
49	chr22:30279000-30281000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr22:30279000-30281200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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