Variant report

Variant	esv1006674
Chromosome Location	chr13:30091232-30095621
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:61)
CpG islands
(count:62)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr13:30095599-30095818	HepG2	liver:	n/a	n/a
2	CTCF	chr13:30095060-30095210	AG10803	skin:	n/a	n/a
3	CTCF	chr13:30094431-30094486	GM13976	blood:	n/a	n/a
4	CTCF	chr13:30094424-30094428	GM13976	blood:	n/a	n/a
5	CTCF	chr13:30095140-30095290	HMF	breast:	n/a	n/a
6	CTCF	chr13:30094940-30095090	NHDF-neo	bronchial:	n/a	n/a
7	CTCF	chr13:30095087-30095191	HUVEC	blood vessel:	n/a	n/a
8	CTCF	chr13:30095040-30095190	HRPEpiC	eye:	n/a	n/a
9	EP300	chr13:30094634-30095470	ECC-1	luminal epithelium:	n/a	n/a
10	EP300	chr13:30094879-30095405	ECC-1	luminal epithelium:	n/a	n/a
11	ESR1	chr13:30094882-30095297	ECC-1	luminal epithelium:	n/a	n/a
12	FOS	chr13:30094863-30095268	HUVEC	blood vessel:	n/a	chr13:30095157-30095166
13	FOSL2	chr13:30094669-30095254	SK-N-SH	brain:	n/a	chr13:30095157-30095166
14	FOXM1	chr13:30094673-30095516	ECC-1	luminal epithelium:	n/a	n/a
15	GATA3	chr13:30094841-30095067	SH-SY5Y	brain:	n/a	n/a
16	JUN	chr13:30094833-30095193	HUVEC	blood vessel:	n/a	chr13:30095157-30095166
17	JUND	chr13:30094754-30095262	SK-N-SH	brain:	n/a	chr13:30095157-30095166
18	NFIC	chr13:30094710-30095533	ECC-1	luminal epithelium:	n/a	n/a
19	NFIC	chr13:30094716-30095471	ECC-1	luminal epithelium:	n/a	n/a
20	NR3C1	chr13:30094895-30095260	ECC-1	luminal epithelium:	n/a	chr13:30095147-30095154
21	NR3C1	chr13:30094900-30095291	ECC-1	luminal epithelium:	n/a	chr13:30095147-30095154
22	POLR2A	chr13:30094962-30101147	K562	blood:	n/a	n/a
23	POLR2A	chr13:30093289-30093435	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr13:30094042-30094389	K562	blood:	n/a	n/a
25	POLR2A	chr13:30095373-30095951	Hela-S3	cervix:	n/a	n/a
26	POLR2A	chr13:30092998-30093796	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr13:30095209-30095456	HUVEC	blood vessel:	n/a	n/a
28	POLR2A	chr13:30091416-30091654	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr13:30094067-30094311	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr13:30094824-30095196	SK-N-SH	brain:	n/a	n/a
31	POLR2A	chr13:30093753-30093759	K562	blood:	n/a	n/a
32	POLR2A	chr13:30095437-30095824	K562	blood:	n/a	n/a
33	POLR2A	chr13:30092781-30092989	K562	blood:	n/a	n/a
34	POLR2A	chr13:30093698-30093930	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr13:30094206-30094425	K562	blood:	n/a	n/a
36	POLR2A	chr13:30079640-30094748	K562	blood:	n/a	n/a
37	POLR2A	chr13:30092119-30092376	K562	blood:	n/a	n/a
38	POLR2A	chr13:30094106-30094686	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr13:30094908-30094947	HUVEC	blood vessel:	n/a	n/a
40	POLR2A	chr13:30093235-30093238	HepG2	liver:	n/a	n/a
41	POLR2A	chr13:30092767-30093302	K562	blood:	n/a	n/a
42	POLR2A	chr13:30093460-30093881	K562	blood:	n/a	n/a
43	POLR2A	chr13:30090731-30091509	K562	blood:	n/a	n/a
44	POLR2A	chr13:30093627-30093653	K562	blood:	n/a	n/a
45	POLR2A	chr13:30090941-30091282	HL-60	blood:	n/a	n/a
46	POLR2A	chr13:30091656-30091701	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr13:30093672-30093711	K562	blood:	n/a	n/a
48	POLR2A	chr13:30093730-30093741	GM12878	blood:	n/a	n/a
49	POLR2A	chr13:30095447-30095909	K562	blood:	n/a	n/a
50	POLR2A	chr13:30090373-30092577	Hela-S3	cervix:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:30092023-30092073	AG09319	gingival:	n/a
2	chr13:30092023-30092073	AG09319	gingival:	n/a
3	chr13:30092023-30092073	K562	blood:	n/a
4	chr13:30092023-30092073	NHBE	bronchial:	n/a
5	chr13:30092023-30092073	U87	brain:	n/a
6	chr13:30092023-30092073	ProgFib	skin:	n/a
7	chr13:30092023-30092073	H1-hESC	embryonic stem cell:	embryo
8	chr13:30092023-30092073	HCT-116	colon:	n/a
9	chr13:30092023-30092073	Hepatocyte	liver:	n/a
10	chr13:30092023-30092073	PrEC	prostate:	n/a
11	chr13:30092023-30092073	SKMC	muscle:	n/a
12	chr13:30092023-30092073	Caco-2	colon:	n/a
13	chr13:30092023-30092073	Jurkat	blood:	n/a
14	chr13:30092023-30092073	A549	lung:	n/a
15	chr13:30092023-30092073	AoSMC	blood vessel:	n/a
16	chr13:30092023-30092073	HEEpiC	esophagus:	n/a
17	chr13:30092023-30092073	BE2_C	brain:	n/a
18	chr13:30092023-30092073	PANC-1	pancreas:	n/a
19	chr13:30092023-30092073	HCF	heart:	n/a
20	chr13:30092023-30092073	HPAEpiC	pulmonary alveolar:	n/a
21	chr13:30092023-30092073	RPTEC	kidney:	n/a
22	chr13:30092023-30092073	HCM	heart:	n/a
23	chr13:30092023-30092073	SK-N-MC	brain:	n/a
24	chr13:30092023-30092073	HepG2	liver:	n/a
25	chr13:30092023-30092073	HUVEC	blood vessel:	n/a
26	chr13:30092023-30092073	HRPEpiC	eye:	n/a
27	chr13:30092023-30092073	HRE	kidney:	n/a
28	chr13:30092023-30092073	AG04450	lung:	fetal
29	chr13:30092023-30092073	LNCaP	prostate:	n/a
30	chr13:30092023-30092073	GM19239	blood:	n/a
31	chr13:30092023-30092073	NB4	blood:	n/a
32	chr13:30092023-30092073	PFSK-1	brain:	n/a
33	chr13:30092023-30092073	GM06990	blood:	n/a
34	chr13:30092023-30092073	SK-N-SH	brain:	n/a
35	chr13:30092023-30092073	ovcar-3	ovarian:	n/a
36	chr13:30092023-30092073	NT2-D1	testis:	n/a
37	chr13:30092023-30092073	MCF10A-Er-Src	breast:	n/a
38	chr13:30092023-30092073	AG09309	skin:	n/a
39	chr13:30092023-30092073	HL-60	blood:	n/a
40	chr13:30092023-30092073	HAEpiC	amniotic membrane:	n/a
41	chr13:30092023-30092073	GM12891	blood:	n/a
42	chr13:30092023-30092073	HNPCEpiC	eye:	n/a
43	chr13:30092023-30092073	HIPEpiC	eye:	n/a
44	chr13:30092023-30092073	MCF-7	breast:	n/a
45	chr13:30092023-30092073	GM12878	blood:	n/a
46	chr13:30092023-30092073	NH-A	brain:	n/a
47	chr13:30092023-30092073	ECC-1	luminal epithelium:	n/a
48	chr13:30092023-30092073	CMK	blood:	n/a
49	chr13:30092023-30092073	IMR90	lung:	fetal
50	chr13:30092023-30092073	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:30090549..30093247-chr13:30094397..30096373,2	K562	blood:
2	chr13:30069216..30072289-chr13:30088515..30091504,3	MCF-7	breast:
3	chr13:30087488..30090042-chr13:30094216..30096567,2	MCF-7	breast:
4	chr13:30082618..30084607-chr13:30095133..30096907,2	K562	blood:
5	chr13:30090549..30093247-chr13:30094397..30096373,2	K562	blood:
6	chr13:30091097..30092804-chr13:30167943..30169459,2	K562	blood:
7	chr13:30086595..30089289-chr13:30090102..30093020,2	K562	blood:
8	chr13:30090549..30094073-chr13:30094397..30097497,3	K562	blood:
9	chr13:30093611..30096522-chr13:30167989..30170777,2	MCF-7	breast:

No data

Variant related genes	Relation type
SLC7A1	TF binding region
SLC7A1	CpG island
ENSG00000139514	chromatin interactions
ENSG00000132938	chromatin interactions

Extended variants
information (count: 178 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:178 , 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	rs567902611	chr13:30091266-30091267	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs372480429	chr13:30091270-30091271	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs141838102	chr13:30091296-30091297	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs370198806	chr13:30091307-30091308	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150624249	chr13:30091308-30091309	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs548607156	chr13:30091325-30091326	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs570378098	chr13:30091329-30091330	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs139952828	chr13:30091338-30091339	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs556791576	chr13:30091361-30091362	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs558914643	chr13:30091362-30091363	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs569947462	chr13:30091384-30091385	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs572309703	chr13:30091412-30091413	Strong transcription Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs535160170	chr13:30091415-30091416	Strong transcription Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs75759022	chr13:30091436-30091437	Strong transcription Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs149857696	chr13:30091437-30091438	Strong transcription Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs373763494	chr13:30091455-30091456	Strong transcription Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs187002131	chr13:30091456-30091457	Strong transcription Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs537003160	chr13:30091473-30091474	Strong transcription Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs563111528	chr13:30091502-30091503	Strong transcription Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs191902091	chr13:30091504-30091505	Strong transcription Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs2490267	chr13:30091516-30091517	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs559337579	chr13:30091553-30091554	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs116766244	chr13:30091554-30091555	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs548949661	chr13:30091576-30091577	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs548331990	chr13:30091618-30091619	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs61495877	chr13:30091638-30091639	Strong transcription Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs371608247	chr13:30091666-30091667	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369729600	chr13:30091675-30091676	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373635088	chr13:30091680-30091681	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370357203	chr13:30091702-30091703	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2482089	chr13:30091714-30091715	Strong transcription Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs375096222	chr13:30091771-30091772	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34072234	chr13:30091775-30091776	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2482090	chr13:30091819-30091820	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs60013611	chr13:30091876-30091877	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs368008310	chr13:30091879-30091880	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144943782	chr13:30091906-30091907	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368572740	chr13:30091940-30091941	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs17602454	chr13:30091946-30091947	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375464757	chr13:30091947-30091948	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552586604	chr13:30091950-30091951	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112149978	chr13:30091952-30091953	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368824362	chr13:30091953-30091954	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116737496	chr13:30091966-30091967	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534688971	chr13:30092024-30092025	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554678944	chr13:30092052-30092053	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574611141	chr13:30092080-30092081	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112250038	chr13:30092081-30092082	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs116573876	chr13:30092101-30092102	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556743783	chr13:30092107-30092108	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	18698080	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Squamous cell cancer	20885788	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Malignant glioma	17146433	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Retinoblastoma	22278416	CNVD
Peters Plus syndrome	16909395	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Ovarian cancer	19047089	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:249 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:30071000-30128800	Strong transcription	Dnd41	blood
2	chr13:30082000-30106600	Weak transcription	Fetal Kidney	kidney
3	chr13:30082000-30107600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr13:30082800-30096000	Weak transcription	Liver	Liver
5	chr13:30082800-30111600	Weak transcription	Stomach Mucosa	stomach
6	chr13:30083200-30107200	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr13:30083600-30094400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr13:30083600-30096400	Weak transcription	Small Intestine	intestine
9	chr13:30084200-30091800	Strong transcription	Placenta Amnion	Placenta Amnion
10	chr13:30084200-30094800	Strong transcription	Thymus	Thymus
11	chr13:30084200-30106000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
12	chr13:30084200-30107800	Strong transcription	Esophagus	oesophagus
13	chr13:30084200-30110400	Strong transcription	Fetal Intestine Small	intestine
14	chr13:30084200-30110600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr13:30084200-30112600	Strong transcription	NHEK	skin
16	chr13:30084200-30115800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr13:30084400-30111200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr13:30084600-30098000	Strong transcription	Rectal Mucosa Donor 29	rectum
19	chr13:30084600-30112200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr13:30084800-30098400	Strong transcription	Gastric	stomach
21	chr13:30084800-30110400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr13:30084800-30110600	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr13:30084800-30111600	Strong transcription	HUES64 Cell Line	embryonic stem cell
24	chr13:30085000-30093800	Strong transcription	Fetal Intestine Large	intestine
25	chr13:30085000-30098600	Strong transcription	Pancreas	Pancrea
26	chr13:30085000-30099000	Strong transcription	H1 Cell Line	embryonic stem cell
27	chr13:30085000-30111600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr13:30085200-30098800	Strong transcription	Duodenum Mucosa	Duodenum
29	chr13:30085200-30099800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr13:30085200-30104200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
31	chr13:30085400-30092200	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr13:30085400-30092600	Weak transcription	Brain Angular Gyrus	brain
33	chr13:30085400-30099800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr13:30085600-30093200	Weak transcription	K562	blood
35	chr13:30085600-30098600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr13:30085600-30098600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
37	chr13:30085600-30098600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
38	chr13:30085600-30111200	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr13:30085600-30111600	Strong transcription	Primary T helper cells PMA-I stimulated	--
40	chr13:30085800-30099400	Strong transcription	Primary T helper cells fromperipheralblood	blood
41	chr13:30085800-30115400	Strong transcription	Primary T cells from cord blood	blood
42	chr13:30086000-30110600	Strong transcription	HUES48 Cell Line	embryonic stem cell
43	chr13:30086000-30111200	Strong transcription	Monocytes-CD14+_RO01746	blood
44	chr13:30086200-30096800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr13:30086400-30092400	Strong transcription	Colonic Mucosa	Colon
46	chr13:30086400-30098600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr13:30086600-30092200	Strong transcription	Colon Smooth Muscle	Colon
48	chr13:30086600-30094000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr13:30086600-30094800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr13:30086600-30095200	Strong transcription	Fetal Thymus	thymus

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