Variant report

Variant	esv274928
Chromosome Location	chr17:37848591-37851632
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:47)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:47 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPD	chr17:37851628-37852144	HepG2	liver:	n/a	n/a
2	CTCF	chr17:37851220-37851370	Caco-2	colon:	n/a	n/a
3	ELF1	chr17:37851589-37852814	HepG2	liver:	n/a	n/a
4	EP300	chr17:37851252-37852535	HepG2	liver:	n/a	n/a
5	EP300	chr17:37851183-37852989	HepG2	liver:	n/a	n/a
6	FOSL2	chr17:37851190-37852663	HepG2	liver:	n/a	chr17:37852641-37852655 chr17:37852422-37852431
7	FOSL2	chr17:37851628-37852266	HepG2	liver:	n/a	n/a
8	FOXA1	chr17:37851289-37852611	HepG2	liver:	n/a	chr17:37851882-37851894
9	FOXA1	chr17:37851602-37852365	HepG2	liver:	n/a	chr17:37851882-37851894
10	FOXA1	chr17:37851586-37852308	HepG2	liver:	n/a	chr17:37851882-37851894
11	FOXA2	chr17:37851466-37852700	HepG2	liver:	n/a	chr17:37851882-37851894
12	HDAC2	chr17:37851337-37852823	HepG2	liver:	n/a	n/a
13	HEY1	chr17:37851184-37852879	HepG2	liver:	n/a	n/a
14	HEY1	chr17:37850909-37852567	HepG2	liver:	n/a	n/a
15	HNF4A	chr17:37851205-37852788	HepG2	liver:	n/a	chr17:37851850-37851865 chr17:37851537-37851559
16	HNF4A	chr17:37851374-37852264	HepG2	liver:	n/a	chr17:37851850-37851865 chr17:37851537-37851559
17	HNF4A	chr17:37851407-37852183	HepG2	liver:	n/a	chr17:37851850-37851865 chr17:37851537-37851559
18	HNF4G	chr17:37851341-37852231	HepG2	liver:	n/a	chr17:37851850-37851865 chr17:37851537-37851559
19	HNF4G	chr17:37851319-37852235	HepG2	liver:	n/a	chr17:37851850-37851865 chr17:37851537-37851559
20	JUND	chr17:37851359-37852478	HepG2	liver:	n/a	chr17:37852422-37852431
21	JUND	chr17:37851383-37851447	H1-hESC	embryonic stem cell:	n/a	n/a
22	MAFK	chr17:37851439-37852336	HepG2	liver:	n/a	n/a
23	MAX	chr17:37851316-37852425	HepG2	liver:	n/a	chr17:37852029-37852038
24	MAZ	chr17:37851538-37852753	HepG2	liver:	n/a	chr17:37852029-37852038 chr17:37852427-37852437
25	MBD4	chr17:37851173-37852558	HepG2	liver:	n/a	n/a
26	MBD4	chr17:37850803-37852434	HepG2	liver:	n/a	n/a
27	MXI1	chr17:37851390-37852732	HepG2	liver:	n/a	n/a
28	MYBL2	chr17:37851089-37853120	HepG2	liver:	n/a	n/a
29	MYBL2	chr17:37851381-37852772	HepG2	liver:	n/a	n/a
30	MYC	chr17:37851522-37851552	HepG2	liver:	n/a	n/a
31	NFIC	chr17:37851361-37852623	HepG2	liver:	n/a	n/a
32	NFIC	chr17:37851220-37852997	HepG2	liver:	n/a	n/a
33	POLR2A	chr17:37851550-37852844	HepG2	liver:	n/a	n/a
34	POLR2A	chr17:37851145-37852824	HepG2	liver:	n/a	n/a
35	POLR2A	chr17:37851013-37852975	HepG2	liver:	n/a	n/a
36	POLR2A	chr17:37851280-37852635	HepG2	liver:	n/a	n/a
37	POLR2A	chr17:37851240-37852695	HepG2	liver:	n/a	n/a
38	POLR2A	chr17:37851191-37852642	HepG2	liver:	n/a	n/a
39	RAD21	chr17:37851627-37852658	HepG2	liver:	n/a	n/a
40	REST	chr17:37851618-37852651	HepG2	liver:	n/a	n/a
41	RFX5	chr17:37851373-37852347	HepG2	liver:	n/a	chr17:37851787-37851796
42	RXRA	chr17:37851511-37852399	HepG2	liver:	n/a	chr17:37852217-37852231
43	RXRA	chr17:37851610-37852278	HepG2	liver:	n/a	chr17:37852217-37852231
44	SP1	chr17:37851174-37852823	HepG2	liver:	n/a	chr17:37852559-37852571 chr17:37852262-37852276 chr17:37852559-37852571 chr17:37852420-37852434 chr17:37852559-37852570 chr17:37851578-37851585 chr17:37852693-37852702
45	TBP	chr17:37851447-37852547	HepG2	liver:	n/a	n/a
46	TEAD4	chr17:37851225-37853069	HepG2	liver:	n/a	n/a
47	YY1	chr17:37851197-37851697	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:37851022-37851072	SK-N-SH_RA	brain:	n/a
2	chr17:37851022-37851072	HAEpiC	amniotic membrane:	n/a
3	chr17:37851022-37851072	IMR90	lung:	fetal
4	chr17:37851022-37851072	AoSMC	blood vessel:	n/a
5	chr17:37851022-37851072	GM12891	blood:	n/a
6	chr17:37851022-37851072	LNCaP	prostate:	n/a
7	chr17:37851022-37851072	HRPEpiC	eye:	n/a
8	chr17:37851022-37851072	SK-N-SH	brain:	n/a
9	chr17:37851022-37851072	HCPEpiC	choroid plexus:	n/a
10	chr17:37851022-37851072	SKMC	muscle:	n/a
11	chr17:37851022-37851072	AG09309	skin:	n/a
12	chr17:37851022-37851072	NT2-D1	testis:	n/a
13	chr17:37851022-37851072	ECC-1	luminal epithelium:	n/a
14	chr17:37851022-37851072	GM06990	blood:	n/a
15	chr17:37851022-37851072	NB4	blood:	n/a
16	chr17:37851022-37851072	BE2_C	brain:	n/a
17	chr17:37851022-37851072	GM12878	blood:	n/a
18	chr17:37851022-37851072	PANC-1	pancreas:	n/a
19	chr17:37851022-37851072	MCF10A-Er-Src	breast:	n/a
20	chr17:37851022-37851072	GM19239	blood:	n/a
21	chr17:37851022-37851072	HCM	heart:	n/a
22	chr17:37851022-37851072	HCT-116	colon:	n/a
23	chr17:37851022-37851072	Hepatocyte	liver:	n/a
24	chr17:37851022-37851072	ovcar-3	ovarian:	n/a
25	chr17:37851022-37851072	ProgFib	skin:	n/a
26	chr17:37851022-37851072	CMK	blood:	n/a
27	chr17:37851022-37851072	T-47D	breast:	n/a
28	chr17:37851022-37851072	HCF	heart:	n/a
29	chr17:37851022-37851072	AG04450	lung:	fetal
30	chr17:37851022-37851072	HRCEpiC	kidney:	n/a
31	chr17:37851022-37851072	U87	brain:	n/a
32	chr17:37851022-37851072	Caco-2	colon:	n/a
33	chr17:37851022-37851072	HUVEC	blood vessel:	n/a
34	chr17:37851022-37851072	HNPCEpiC	eye:	n/a
35	chr17:37851022-37851072	HL-60	blood:	n/a
36	chr17:37851022-37851072	PrEC	prostate:	n/a
37	chr17:37851022-37851072	HEK293	kidney:	embryo
38	chr17:37851022-37851072	Jurkat	blood:	n/a
39	chr17:37851022-37851072	AG09319	gingival:	n/a
40	chr17:37851022-37851072	A549	lung:	n/a
41	chr17:37851022-37851072	MCF-7	breast:	n/a
42	chr17:37851022-37851072	Hela-S3	cervix:	n/a
43	chr17:37851022-37851072	PFSK-1	brain:	n/a
44	chr17:37851022-37851072	AG10803	skin:	n/a
45	chr17:37851022-37851072	AG04449	skin:	fetal
46	chr17:37851022-37851072	NH-A	brain:	n/a
47	chr17:37851022-37851072	SK-N-MC	brain:	n/a
48	chr17:37851022-37851072	K562	blood:	n/a
49	chr17:37851022-37851072	NHBE	bronchial:	n/a
50	chr17:37851022-37851072	GM12892	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr17:37847911..37850678-chr17:37853588..37855984,2	K562	blood:
2	chr17:37842900..37846348-chr17:37848501..37850475,3	K562	blood:
3	chr17:37775565..37777300-chr17:37849903..37852846,2	K562	blood:
4	chr17:37842383..37849519-chr17:37854521..37862509,17	MCF-7	breast:
5	chr17:37851119..37852804-chr17:37855350..37857292,2	MCF-7	breast:
6	chr17:37843961..37847165-chr17:37847393..37849568,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ERBB2-1	chr17:37850934-37851434	NONHSAT053467
2	lnc-ERBB2-1	chr17:37849514-37849578	NONHSAT053467

No data

Variant related genes	Relation type
PGAP3	TF binding region
ERBB2	TF binding region
PGAP3	CpG island
ERBB2	CpG island
ENSG00000141736	chromatin interactions
ENSG00000161395	chromatin interactions
ENSG00000214546	chromatin interactions

Extended variants
information (count: 109 )
Associated
traits (count: 130 )

Variant overlapped rSNPs/rCNVs (count:109 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566653779	chr17:37848612-37848613	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs371884549	chr17:37848616-37848617	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs374405459	chr17:37848641-37848642	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs567443656	chr17:37848642-37848643	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs77155727	chr17:37848674-37848675	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs375364772	chr17:37848675-37848676	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs377005420	chr17:37848676-37848677	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs2904766	chr17:37848677-37848678	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs572656035	chr17:37848684-37848685	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs560912894	chr17:37848693-37848694	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs368015113	chr17:37848719-37848720	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs187123502	chr17:37848720-37848721	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs544866060	chr17:37848721-37848722	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs554202128	chr17:37848749-37848750	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs371707194	chr17:37848762-37848763	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs191945396	chr17:37848782-37848783	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs561729631	chr17:37848807-37848808	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs529653937	chr17:37848808-37848809	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs142146683	chr17:37848818-37848819	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs544182296	chr17:37848821-37848822	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs562467135	chr17:37848901-37848902	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs144771873	chr17:37848904-37848905	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs374704654	chr17:37848937-37848938	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs551640346	chr17:37848938-37848939	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs116423875	chr17:37848989-37848990	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs527454166	chr17:37848990-37848991	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs548782862	chr17:37849003-37849004	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs567383956	chr17:37849032-37849033	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs549656303	chr17:37849078-37849079	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs148433544	chr17:37849085-37849086	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs566083038	chr17:37849087-37849088	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs571290538	chr17:37849088-37849089	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs538684982	chr17:37849119-37849120	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs554415458	chr17:37849133-37849134	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs528445337	chr17:37849136-37849137	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs551867044	chr17:37849151-37849152	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs543164667	chr17:37849255-37849256	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs571682649	chr17:37849261-37849262	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs555206093	chr17:37849308-37849309	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs576759858	chr17:37849367-37849368	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs368891242	chr17:37849381-37849382	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs562609960	chr17:37849388-37849389	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs142555407	chr17:37849455-37849456	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs77509884	chr17:37849505-37849506	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs187431136	chr17:37849576-37849577	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs537533029	chr17:37849580-37849581	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs527602200	chr17:37849668-37849669	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs150938343	chr17:37849773-37849774	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs560738693	chr17:37849844-37849845	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs567116661	chr17:37849916-37849917	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:130)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17157792	CNVD
Bladder cancer	19088036	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Meningioma	19431122	CNVD
Neurocytoma	17123091	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	24379144	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	17850661	CNVD
Primary lung adenocarcinoma	16799635	CNVD
HIV/AIDS	18848619	CNVD
Rheumatoid arthritis	19220326	CNVD
Rheumatoid arthritis	18848619	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	18848619	CNVD
Type 1 diabetes	19220326	CNVD
HIV/AIDS	17330138	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Acute monocytic leukemia	16498392	CNVD
Breast cancer	20409316	CNVD
Myelodysplastic syndrome	18663149	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164920	CNVD
Urothelial carcinoma	21177765	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Disease	22962312	CNVD
Mental retardation	20152051	CNVD
Mental retardation	19951919	CNVD
Mental retardation	22817714	CNVD
Mental retardation	21956041	CNVD
Brain cancer	19584924	CNVD
Glioblastoma multiforme	22286061	CNVD
Schizophrenia	21399695	CNVD
Non-syndromic sensorineural hearing loss	19165922	CNVD
Prader-willi syndrome	20588305	CNVD
17q21.31 microdeletion syndrome	16940994	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
17q21.31 microdeletion syndrome	22283845	CNVD
Intellectual disability	22194194	CNVD
17q21.31 microdeletion syndrome	20606400	CNVD
17q21.31 microdeletion syndrome	18628315	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	18702822	CNVD
Breast cancer	17938205	CNVD
Breast cancer	20943603	CNVD
Pheochromocytoma	18310300	CNVD
Gastric adenocarcinoma	22014070	CNVD

Chromatin state (count:151 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37845000-37856000	Weak transcription	Lung	lung
2	chr17:37845200-37854600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr17:37845200-37854600	Weak transcription	Brain Hippocampus Middle	brain
4	chr17:37845400-37849800	Weak transcription	Brain Angular Gyrus	brain
5	chr17:37845400-37850800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr17:37845400-37850800	Weak transcription	Duodenum Mucosa	Duodenum
7	chr17:37845400-37850800	Weak transcription	Fetal Kidney	kidney
8	chr17:37845400-37850800	Weak transcription	Fetal Stomach	stomach
9	chr17:37845400-37851000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr17:37845400-37851000	Weak transcription	Colonic Mucosa	Colon
11	chr17:37845400-37851000	Weak transcription	Fetal Muscle Trunk	muscle
12	chr17:37845400-37851200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr17:37845400-37851600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr17:37845400-37854800	Weak transcription	Placenta	Placenta
15	chr17:37845400-37855000	Weak transcription	Brain Substantia Nigra	brain
16	chr17:37845400-37855400	Weak transcription	Left Ventricle	heart
17	chr17:37845400-37855800	Weak transcription	Aorta	Aorta
18	chr17:37845600-37850200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr17:37845600-37850800	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr17:37845600-37851000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr17:37845600-37851000	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr17:37845600-37851000	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr17:37845600-37851200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr17:37845600-37851200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr17:37845600-37851200	Weak transcription	Fetal Lung	lung
26	chr17:37845600-37851400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr17:37845600-37851400	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr17:37845600-37851400	Weak transcription	Stomach Mucosa	stomach
29	chr17:37845600-37852000	Weak transcription	Pancreas	Pancrea
30	chr17:37845600-37852200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr17:37845600-37852800	Weak transcription	Primary B cells from peripheral blood	blood
32	chr17:37845600-37853400	Weak transcription	Primary hematopoietic stem cells	blood
33	chr17:37845600-37854600	Weak transcription	Primary B cells from cord blood	blood
34	chr17:37845600-37855000	Weak transcription	Fetal Brain Female	brain
35	chr17:37845600-37855400	Weak transcription	Colon Smooth Muscle	Colon
36	chr17:37845600-37855800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr17:37845600-37855800	Weak transcription	Ovary	ovary
38	chr17:37845600-37855800	Weak transcription	Psoas Muscle	Psoas
39	chr17:37845600-37855800	Weak transcription	Right Ventricle	heart
40	chr17:37845600-37855800	Weak transcription	HSMMtube	muscle
41	chr17:37845600-37856000	Weak transcription	Esophagus	oesophagus
42	chr17:37845600-37856000	Weak transcription	Spleen	Spleen
43	chr17:37845800-37848600	Weak transcription	Fetal Intestine Small	intestine
44	chr17:37845800-37848800	Weak transcription	Fetal Intestine Large	intestine
45	chr17:37845800-37850600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr17:37845800-37850600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr17:37845800-37850800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr17:37845800-37850800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr17:37845800-37850800	Weak transcription	Brain Anterior Caudate	brain
50	chr17:37845800-37850800	Weak transcription	Rectal Mucosa Donor 31	rectum

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