Variant report

Variant	esv20134
Chromosome Location	chr3:195673006-195720655
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1614)
CpG islands
(count:1709)
Chromatin interactive
region (count:14)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1614 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:195687778-195688031	K562	blood:	n/a	n/a
2	ATF1	chr3:195681353-195681596	K562	blood:	n/a	n/a
3	ATF2	chr3:195681259-195681587	GM12878	blood:	n/a	n/a
4	ATF3	chr3:195717483-195717694	K562	blood:	n/a	n/a
5	ATF3	chr3:195681303-195681452	K562	blood:	n/a	n/a
6	ATF3	chr3:195717064-195717382	K562	blood:	n/a	n/a
7	ATF3	chr3:195678739-195678871	K562	blood:	n/a	n/a
8	ATF3	chr3:195717164-195717371	K562	blood:	n/a	n/a
9	ATF3	chr3:195717067-195717371	A549	lung:	n/a	n/a
10	BACH1	chr3:195717045-195717538	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr3:195680472-195680694	GM12878	blood:	n/a	n/a
12	BATF	chr3:195715731-195716052	GM12878	blood:	n/a	n/a
13	BATF	chr3:195716145-195716590	GM12878	blood:	n/a	n/a
14	BATF	chr3:195705475-195705667	GM12878	blood:	n/a	chr3:195705640-195705649 chr3:195705599-195705610
15	BATF	chr3:195717279-195717490	GM12878	blood:	n/a	n/a
16	BATF	chr3:195688640-195688926	GM12878	blood:	n/a	n/a
17	BATF	chr3:195681129-195681669	GM12878	blood:	n/a	n/a
18	BATF	chr3:195682771-195683491	GM12878	blood:	n/a	n/a
19	BATF	chr3:195681681-195681957	GM12878	blood:	n/a	n/a
20	BATF	chr3:195682768-195683488	GM12878	blood:	n/a	n/a
21	BATF	chr3:195717540-195717834	GM12878	blood:	n/a	n/a
22	BCL11A	chr3:195680538-195680860	GM12878	blood:	n/a	chr3:195680659-195680668
23	BCL11A	chr3:195679579-195679786	GM12878	blood:	n/a	chr3:195679673-195679680
24	BCL11A	chr3:195682872-195683277	GM12878	blood:	n/a	n/a
25	BCL11A	chr3:195680283-195680924	GM12878	blood:	n/a	chr3:195680659-195680668
26	BCL11A	chr3:195681118-195681900	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
27	BCL11A	chr3:195717296-195717514	GM12878	blood:	n/a	chr3:195717473-195717482
28	BCL11A	chr3:195711556-195711737	GM12878	blood:	n/a	n/a
29	BCL11A	chr3:195681860-195682057	GM12878	blood:	n/a	n/a
30	BCL11A	chr3:195716071-195717206	GM12878	blood:	n/a	chr3:195716811-195716824 chr3:195716792-195716801 chr3:195716946-195716959
31	BCL11A	chr3:195715512-195715842	GM12878	blood:	n/a	n/a
32	BCL11A	chr3:195679437-195679731	GM12878	blood:	n/a	chr3:195679673-195679680
33	BCL11A	chr3:195717225-195717865	GM12878	blood:	n/a	chr3:195717473-195717482
34	BCL11A	chr3:195681171-195681812	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
35	BCL11A	chr3:195682895-195683356	GM12878	blood:	n/a	n/a
36	BCL3	chr3:195681285-195681563	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
37	BCL3	chr3:195700608-195700811	GM12878	blood:	n/a	n/a
38	BCLAF1	chr3:195681279-195681563	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
39	BCLAF1	chr3:195681253-195681686	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
40	BHLHE40	chr3:195717520-195717617	K562	blood:	n/a	n/a
41	BHLHE40	chr3:195681214-195681663	GM12878	blood:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
42	BHLHE40	chr3:195717244-195717251	K562	blood:	n/a	n/a
43	BHLHE40	chr3:195681210-195681587	K562	blood:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
44	BHLHE40	chr3:195681203-195681678	HepG2	liver:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
45	BRCA1	chr3:195681377-195681604	Hela-S3	cervix:	n/a	n/a
46	CBX3	chr3:195717317-195717855	K562	blood:	n/a	n/a
47	CBX3	chr3:195679046-195679922	K562	blood:	n/a	n/a
48	CBX3	chr3:195681209-195681715	K562	blood:	n/a	n/a
49	CBX3	chr3:195681152-195682264	K562	blood:	n/a	n/a
50	CBX3	chr3:195716251-195717942	K562	blood:	n/a	n/a

(count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195719790-195719840	SAEC	small airway:	n/a
2	chr3:195719790-195719840	SAEC	small airway:	n/a
3	chr3:195678176-195678226	PrEC	prostate:	n/a
4	chr3:195679450-195679500	GM06990	blood:	n/a
5	chr3:195701166-195701216	NB4	blood:	n/a
6	chr3:195701118-195701168	IMR90	lung:	fetal
7	chr3:195688021-195688071	GM06990	blood:	n/a
8	chr3:195717416-195717466	NH-A	brain:	n/a
9	chr3:195715851-195715901	HNPCEpiC	eye:	n/a
10	chr3:195688021-195688071	PANC-1	pancreas:	n/a
11	chr3:195703920-195703970	CMK	blood:	n/a
12	chr3:195717574-195717624	AoSMC	blood vessel:	n/a
13	chr3:195717574-195717624	BE2_C	brain:	n/a
14	chr3:195681091-195681141	NHDF-neo	bronchial:	n/a
15	chr3:195717344-195717394	Hela-S3	cervix:	n/a
16	chr3:195719262-195719312	HRPEpiC	eye:	n/a
17	chr3:195709661-195709711	GM12878	blood:	n/a
18	chr3:195717344-195717394	GM12878	blood:	n/a
19	chr3:195681400-195681450	AG09309	skin:	n/a
20	chr3:195717574-195717624	PFSK-1	brain:	n/a
21	chr3:195683635-195683685	Hela-S3	cervix:	n/a
22	chr3:195714100-195714150	AG10803	skin:	n/a
23	chr3:195709715-195709765	PANC-1	pancreas:	n/a
24	chr3:195717962-195718012	ECC-1	luminal epithelium:	n/a
25	chr3:195717416-195717466	T-47D	breast:	n/a
26	chr3:195709715-195709765	BJ	skin:	n/a
27	chr3:195678176-195678226	BJ	skin:	n/a
28	chr3:195701166-195701216	HCF	heart:	n/a
29	chr3:195714100-195714150	MCF-7	breast:	n/a
30	chr3:195715851-195715901	HCT-116	colon:	n/a
31	chr3:195717574-195717624	NH-A	brain:	n/a
32	chr3:195682365-195682415	LNCaP	prostate:	n/a
33	chr3:195717366-195717416	A549	lung:	n/a
34	chr3:195700735-195700785	U87	brain:	n/a
35	chr3:195700735-195700785	GM12878	blood:	n/a
36	chr3:195688021-195688071	HNPCEpiC	eye:	n/a
37	chr3:195701166-195701216	GM12878	blood:	n/a
38	chr3:195716626-195716676	NH-A	brain:	n/a
39	chr3:195701166-195701216	BJ	skin:	n/a
40	chr3:195683635-195683685	AoSMC	blood vessel:	n/a
41	chr3:195682365-195682415	PANC-1	pancreas:	n/a
42	chr3:195715851-195715901	HEK293	kidney:	embryo
43	chr3:195709661-195709711	AG09309	skin:	n/a
44	chr3:195717574-195717624	HEK293	kidney:	embryo
45	chr3:195703920-195703970	AG10803	skin:	n/a
46	chr3:195681091-195681141	HRCEpiC	kidney:	n/a
47	chr3:195714100-195714150	HIPEpiC	eye:	n/a
48	chr3:195682365-195682415	AoSMC	blood vessel:	n/a
49	chr3:195709715-195709765	HL-60	blood:	n/a
50	chr3:195688021-195688071	BE2_C	brain:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:195361732..195362263-chr3:195681373..195681896,2	MCF-7	breast:
2	chr3:195645901..195648267-chr3:195679890..195681479,3	MCF-7	breast:
3	chr3:195384344..195385079-chr3:195717098..195717747,2	MCF-7	breast:
4	chr3:195679874..195682569-chr3:197381110..197382679,2	K562	blood:
5	chr3:195636473..195638760-chr3:195679951..195681488,2	MCF-7	breast:
6	chr3:195384346..195385021-chr3:195716746..195717598,2	HCT-116	colon:
7	chr3:195416074..195419636-chr3:195682871..195685500,3	K562	blood:
8	chr3:195639677..195641924-chr3:195679365..195681428,2	MCF-7	breast:
9	chr3:195361738..195362245-chr3:195681393..195681916,2	HCT-116	colon:
10	chr3:195419233..195421889-chr3:195682348..195684419,2	K562	blood:
11	chr3:195673861..195675995-chr5:278201..279705,3	K562	blood:
12	chr3:195679870..195682569-chr3:197379763..197382610,2	K562	blood:
13	chr3:195620748..195623055-chr3:195679886..195681403,2	K562	blood:
14	chr3:195620748..195623057-chr3:195678515..195681386,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNK2-2	chr3:195673684-195674350	NONHSAT094275
2	lnc-TNK2-2	chr3:195674206-195674576	NONHSAT094271
3	lnc-TNK2-6	chr3:195688656-195689069	expReg_chr3_13675_-
4	lnc-TNK2-2	chr3:195676113-195676284	NONHSAT094275
5	lnc-MUC20-9	chr3:195674996-195675559	NONHSAT094276
6	lnc-TNK2-2	chr3:195676059-195679566	ENSG00000260261.1

No data

Variant related genes	Relation type
SDHAP1	TF binding region
ENSG00000231464	TF binding region
ENSG00000260261	TF binding region
SDHAP1	CpG island
ENSG00000231464	CpG island
ENSG00000260261	CpG island
ENSG00000061938	chromatin interactions
ENSG00000229178	chromatin interactions
ENSG00000266730	chromatin interactions
ENSG00000242086	chromatin interactions
ENSG00000215837	chromatin interactions
ENSG00000273009	chromatin interactions

Extended variants
information (count: 2486 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2486 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12374200	chr3:195673023-195673024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs547076205	chr3:195673026-195673027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs4459933	chr3:195673043-195673044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs12489052	chr3:195673049-195673050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150242693	chr3:195673060-195673061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531772335	chr3:195673062-195673063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543636085	chr3:195673070-195673071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs4475069	chr3:195673078-195673079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs9835706	chr3:195673106-195673107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4588400	chr3:195673107-195673108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570214925	chr3:195673112-195673113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2928362	chr3:195673123-195673124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs58167810	chr3:195673155-195673156	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs556136860	chr3:195673156-195673157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4446242	chr3:195673181-195673182	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
16	rs12487851	chr3:195673221-195673222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12485275	chr3:195673237-195673238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs9823872	chr3:195673243-195673244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs4475070	chr3:195673278-195673279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs199840107	chr3:195673284-195673285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs574246130	chr3:195673343-195673344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535045408	chr3:195673345-195673346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9827644	chr3:195673353-195673354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4927863	chr3:195673376-195673377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs4927862	chr3:195673399-195673400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs62285293	chr3:195673452-195673453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs147106568	chr3:195673453-195673454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1679295	chr3:195673470-195673471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183279789	chr3:195673491-195673492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566463514	chr3:195673501-195673502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563942760	chr3:195673508-195673509	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78789590	chr3:195673524-195673525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187811812	chr3:195673525-195673526	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs193167538	chr3:195673532-195673533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549311416	chr3:195673536-195673537	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185051450	chr3:195673539-195673540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs62285294	chr3:195673540-195673541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575794699	chr3:195673543-195673544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs4037317	chr3:195673557-195673558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200325964	chr3:195673559-195673560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201007950	chr3:195673563-195673564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377095759	chr3:195673564-195673565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs374995878	chr3:195673574-195673575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs538038772	chr3:195673576-195673577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs199745169	chr3:195673607-195673608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371463960	chr3:195673639-195673640	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374734298	chr3:195673642-195673643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113344171	chr3:195673663-195673664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368461247	chr3:195673712-195673713	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs28759193	chr3:195673738-195673739	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	mRNA abundance

Variant related diseases (count:83)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1911 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195647200-195681200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr3:195648600-195680600	Weak transcription	Pancreas	Pancrea
3	chr3:195651800-195673800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr3:195656600-195681000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr3:195656800-195676400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr3:195656800-195679400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr3:195657800-195681400	Weak transcription	GM12878-XiMat	blood
8	chr3:195659000-195676400	Weak transcription	Hela-S3	cervix
9	chr3:195659600-195681200	Weak transcription	Brain Hippocampus Middle	brain
10	chr3:195659600-195685600	Weak transcription	Small Intestine	intestine
11	chr3:195660000-195681200	Weak transcription	Colonic Mucosa	Colon
12	chr3:195660400-195680600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr3:195660600-195681200	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr3:195661200-195681000	Weak transcription	Ovary	ovary
15	chr3:195661800-195681200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr3:195663400-195681200	Weak transcription	Left Ventricle	heart
17	chr3:195663600-195673800	Weak transcription	Liver	Liver
18	chr3:195663600-195681000	Weak transcription	Fetal Brain Female	brain
19	chr3:195663600-195681200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr3:195663600-195681200	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr3:195663800-195682000	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr3:195664400-195681200	Weak transcription	Osteobl	bone
23	chr3:195665000-195681200	Weak transcription	Placenta	Placenta
24	chr3:195665200-195677800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr3:195665200-195691800	Weak transcription	HSMMtube	muscle
26	chr3:195665400-195681400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr3:195665400-195685200	Weak transcription	Aorta	Aorta
28	chr3:195666000-195673200	Weak transcription	Primary B cells from cord blood	blood
29	chr3:195666000-195677200	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr3:195666000-195677800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr3:195667200-195681200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr3:195667400-195677200	Weak transcription	Gastric	stomach
33	chr3:195667400-195677200	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr3:195667400-195680800	Weak transcription	Right Ventricle	heart
35	chr3:195667400-195681200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr3:195667400-195681200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr3:195667400-195681200	Weak transcription	Brain Anterior Caudate	brain
38	chr3:195667400-195681200	Weak transcription	Brain Cingulate Gyrus	brain
39	chr3:195667400-195681200	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr3:195667400-195681200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr3:195667400-195681400	Weak transcription	Primary B cells from peripheral blood	blood
42	chr3:195667400-195681400	Weak transcription	Brain Substantia Nigra	brain
43	chr3:195667400-195684200	Weak transcription	Spleen	Spleen
44	chr3:195667400-195686200	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr3:195667600-195677600	Weak transcription	Primary T cells from cord blood	blood
46	chr3:195667600-195680200	Weak transcription	Fetal Stomach	stomach
47	chr3:195667600-195681200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr3:195667600-195681200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr3:195667600-195681200	Weak transcription	Esophagus	oesophagus
50	chr3:195667600-195681400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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