Variant report

Variant	esv1792410
Chromosome Location	chr19:42768288-42773316
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:42772131-42772978	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:42772016-42773501	K562	blood:	n/a	n/a
3	ATF1	chr19:42771939-42773502	K562	blood:	n/a	n/a
4	ATF2	chr19:42771955-42773447	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr19:42772114-42773441	GM12878	blood:	n/a	n/a
6	ATF2	chr19:42772120-42773434	GM12878	blood:	n/a	n/a
7	ATF2	chr19:42771881-42773338	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr19:42772414-42773029	K562	blood:	n/a	chr19:42772602-42772615 chr19:42772828-42772836
9	ATF3	chr19:42771594-42773486	A549	lung:	n/a	chr19:42772602-42772615 chr19:42773461-42773470 chr19:42773235-42773244 chr19:42772828-42772836
10	ATF3	chr19:42771750-42773329	A549	lung:	n/a	chr19:42772602-42772615 chr19:42773235-42773244 chr19:42772828-42772836
11	ATF3	chr19:42772107-42772785	K562	blood:	n/a	chr19:42772602-42772615
12	BACH1	chr19:42772085-42772578	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr19:42772240-42772440	K562	blood:	n/a	n/a
14	BATF	chr19:42772347-42772644	GM12878	blood:	n/a	n/a
15	BCL11A	chr19:42772351-42772700	GM12878	blood:	n/a	n/a
16	BCL3	chr19:42771589-42773592	A549	lung:	n/a	chr19:42773504-42773513 chr19:42773235-42773248
17	BCL3	chr19:42771554-42773882	A549	lung:	n/a	chr19:42773504-42773513 chr19:42773235-42773248
18	BCLAF1	chr19:42772340-42773076	GM12878	blood:	n/a	n/a
19	BHLHE40	chr19:42772392-42773434	GM12878	blood:	n/a	chr19:42772619-42772635
20	BHLHE40	chr19:42771857-42773384	K562	blood:	n/a	chr19:42772619-42772635
21	BRCA1	chr19:42772472-42773396	GM12878	blood:	n/a	n/a
22	BRCA1	chr19:42772442-42772673	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr19:42772469-42773401	HepG2	liver:	n/a	n/a
24	BRCA1	chr19:42772319-42773452	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr19:42772058-42772254	GM12878	blood:	n/a	n/a
26	CBX3	chr19:42772206-42773477	K562	blood:	n/a	n/a
27	CCNT2	chr19:42772180-42773522	K562	blood:	n/a	chr19:42772524-42772533 chr19:42773461-42773470 chr19:42772578-42772587 chr19:42773235-42773244
28	CEBPB	chr19:42771492-42773567	A549	lung:	n/a	chr19:42773027-42773035 chr19:42772634-42772642 chr19:42773367-42773375 chr19:42772483-42772491
29	CEBPB	chr19:42769350-42769544	A549	lung:	n/a	chr19:42769418-42769429
30	CEBPB	chr19:42769379-42769495	K562	blood:	n/a	chr19:42769418-42769429
31	CEBPB	chr19:42769349-42769574	HepG2	liver:	n/a	chr19:42769418-42769429
32	CEBPB	chr19:42772059-42772727	H1-hESC	embryonic stem cell:	n/a	chr19:42772634-42772642 chr19:42772483-42772491
33	CEBPB	chr19:42771417-42773461	A549	lung:	n/a	chr19:42773027-42773035 chr19:42772634-42772642 chr19:42773367-42773375 chr19:42772483-42772491
34	CEBPB	chr19:42772131-42772967	K562	blood:	n/a	chr19:42772634-42772642 chr19:42772483-42772491
35	CEBPB	chr19:42771385-42773002	K562	blood:	n/a	chr19:42772634-42772642 chr19:42772483-42772491
36	CEBPB	chr19:42771394-42772789	HepG2	liver:	n/a	chr19:42772634-42772642 chr19:42772483-42772491
37	CEBPB	chr19:42771498-42772799	IMR90	lung:	n/a	chr19:42772634-42772642 chr19:42772483-42772491
38	CEBPB	chr19:42771396-42771756	K562	blood:	n/a	n/a
39	CEBPB	chr19:42772097-42773410	Hela-S3	cervix:	n/a	chr19:42773027-42773035 chr19:42772634-42772642 chr19:42773367-42773375 chr19:42772483-42772491
40	CEBPD	chr19:42772183-42772539	HepG2	liver:	n/a	chr19:42772238-42772249
41	CEBPD	chr19:42773262-42773570	HepG2	liver:	n/a	n/a
42	CEBPZ	chr19:42772702-42773550	HepG2	liver:	n/a	n/a
43	CHD1	chr19:42772241-42772954	GM12878	blood:	n/a	n/a
44	CHD2	chr19:42772282-42773557	GM12878	blood:	n/a	chr19:42773462-42773472
45	CHD2	chr19:42772014-42773588	Hela-S3	cervix:	n/a	chr19:42773462-42773472
46	CHD2	chr19:42772322-42773566	H1-hESC	embryonic stem cell:	n/a	chr19:42773462-42773472
47	CHD2	chr19:42772328-42773508	HepG2	liver:	n/a	chr19:42773462-42773472
48	CHD2	chr19:42772264-42773555	K562	blood:	n/a	chr19:42773462-42773472
49	CREB1	chr19:42772393-42773577	ECC-1	luminal epithelium:	n/a	n/a
50	CREB1	chr19:42772019-42773619	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:42772446-42772496	HIPEpiC	eye:	n/a
2	chr19:42772446-42772496	HIPEpiC	eye:	n/a
3	chr19:42772831-42772881	ProgFib	skin:	n/a
4	chr19:42772233-42772283	H1-hESC	embryonic stem cell:	embryo
5	chr19:42772831-42772881	SAEC	small airway:	n/a
6	chr19:42772446-42772496	ECC-1	luminal epithelium:	n/a
7	chr19:42772831-42772881	NHDF-neo	bronchial:	n/a
8	chr19:42772233-42772283	NHDF-neo	bronchial:	n/a
9	chr19:42772233-42772283	HRPEpiC	eye:	n/a
10	chr19:42772233-42772283	HIPEpiC	eye:	n/a
11	chr19:42772892-42772942	HRE	kidney:	n/a
12	chr19:42768724-42768774	HEK293	kidney:	embryo
13	chr19:42768724-42768774	PFSK-1	brain:	n/a
14	chr19:42772233-42772283	AG10803	skin:	n/a
15	chr19:42772892-42772942	Jurkat	blood:	n/a
16	chr19:42772446-42772496	HMEC	breast:	n/a
17	chr19:42772233-42772283	GM12891	blood:	n/a
18	chr19:42772446-42772496	BJ	skin:	n/a
19	chr19:42772233-42772283	T-47D	breast:	n/a
20	chr19:42772233-42772283	HCT-116	colon:	n/a
21	chr19:42772892-42772942	HRPEpiC	eye:	n/a
22	chr19:42772233-42772283	GM12878	blood:	n/a
23	chr19:42772446-42772496	HepG2	liver:	n/a
24	chr19:42772233-42772283	ProgFib	skin:	n/a
25	chr19:42772446-42772496	HEK293	kidney:	embryo
26	chr19:42772446-42772496	IMR90	lung:	fetal
27	chr19:42772446-42772496	NHDF-neo	bronchial:	n/a
28	chr19:42772233-42772283	AG09309	skin:	n/a
29	chr19:42772446-42772496	HEEpiC	esophagus:	n/a
30	chr19:42772233-42772283	AoSMC	blood vessel:	n/a
31	chr19:42772233-42772283	NB4	blood:	n/a
32	chr19:42768724-42768774	K562	blood:	n/a
33	chr19:42772831-42772881	Hela-S3	cervix:	n/a
34	chr19:42772831-42772881	HCPEpiC	choroid plexus:	n/a
35	chr19:42772892-42772942	AG10803	skin:	n/a
36	chr19:42772892-42772942	HL-60	blood:	n/a
37	chr19:42772831-42772881	HUVEC	blood vessel:	n/a
38	chr19:42772892-42772942	T-47D	breast:	n/a
39	chr19:42772446-42772496	Hela-S3	cervix:	n/a
40	chr19:42772892-42772942	ProgFib	skin:	n/a
41	chr19:42772831-42772881	NH-A	brain:	n/a
42	chr19:42768724-42768774	ECC-1	luminal epithelium:	n/a
43	chr19:42768724-42768774	AG04449	skin:	fetal
44	chr19:42772233-42772283	HL-60	blood:	n/a
45	chr19:42772446-42772496	HL-60	blood:	n/a
46	chr19:42772892-42772942	NHDF-neo	bronchial:	n/a
47	chr19:42772446-42772496	LNCaP	prostate:	n/a
48	chr19:42772892-42772942	SK-N-SH_RA	brain:	n/a
49	chr19:42772831-42772881	K562	blood:	n/a
50	chr19:42772233-42772283	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:42768481..42770570-chr19:42770967..42773649,2	K562	blood:
2	chr19:42720638..42724432-chr19:42771891..42775014,4	MCF-7	breast:
3	chr19:42771398..42774307-chr19:42804493..42807877,4	MCF-7	breast:
4	chr19:42764600..42766454-chr19:42770815..42772327,3	MCF-7	breast:
5	chr19:42771105..42773106-chr19:42805155..42808634,5	K562	blood:
6	chr19:42747132..42763787-chr19:42768368..42776785,67	MCF-7	breast:

Variant related genes	Relation type
CIC	TF binding region
CIC	CpG island
ENSG00000160570	chromatin interactions
ENSG00000268643	chromatin interactions
ENSG00000079432	chromatin interactions
ENSG00000188368	chromatin interactions
ENSG00000105722	chromatin interactions
ENSG00000079462	chromatin interactions
ENSG00000167625	chromatin interactions

Extended variants
information (count: 178 )
Associated
traits (count: 64 )

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	rs34081629	chr19:42768288-42768289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559083563	chr19:42768289-42768290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528809820	chr19:42768291-42768292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184692900	chr19:42768323-42768324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375269539	chr19:42768335-42768336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145255764	chr19:42768397-42768398	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs542475270	chr19:42768453-42768454	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs554347584	chr19:42768500-42768501	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs115957604	chr19:42768514-42768515	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs543536960	chr19:42768515-42768516	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs55678000	chr19:42768573-42768574	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs55973631	chr19:42768588-42768589	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs564807156	chr19:42768598-42768599	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs557432901	chr19:42768614-42768615	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs369091312	chr19:42768701-42768702	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs541041061	chr19:42768743-42768744	Weak transcription	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs111816360	chr19:42768754-42768755	Weak transcription	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs117359636	chr19:42768770-42768771	Weak transcription	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs559293181	chr19:42768793-42768794	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs529443055	chr19:42768796-42768797	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs189360457	chr19:42768885-42768886	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs76406904	chr19:42768891-42768892	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs111523289	chr19:42768919-42768920	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs531799489	chr19:42768923-42768924	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs548585337	chr19:42768924-42768925	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs372902670	chr19:42768974-42768975	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs568016936	chr19:42768975-42768976	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs550279248	chr19:42768995-42768996	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs112668431	chr19:42769010-42769011	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs539089549	chr19:42769021-42769022	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs202101974	chr19:42769058-42769059	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs547397347	chr19:42769066-42769067	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs535534102	chr19:42769079-42769080	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs565690882	chr19:42769088-42769089	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs200420836	chr19:42769111-42769112	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs553628075	chr19:42769128-42769129	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs572055019	chr19:42769155-42769156	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs369841967	chr19:42769181-42769182	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs113379280	chr19:42769209-42769210	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs543375596	chr19:42769247-42769248	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs576871414	chr19:42769254-42769255	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs541078168	chr19:42769258-42769259	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs559435986	chr19:42769265-42769266	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs574478735	chr19:42769284-42769285	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs543379307	chr19:42769296-42769297	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs191379591	chr19:42769299-42769300	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs532005848	chr19:42769311-42769312	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs550122864	chr19:42769315-42769316	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs556885647	chr19:42769316-42769317	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs373998719	chr19:42769336-42769337	Weak transcription	Chromatin interactive region	3 gene(s)	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
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	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
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Autism	20841430	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42760400-42771800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr19:42761400-42771800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr19:42761800-42771800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr19:42762800-42771800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr19:42763400-42771600	Weak transcription	K562	blood
6	chr19:42763400-42771800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr19:42764600-42771800	Weak transcription	Duodenum Mucosa	Duodenum
8	chr19:42766400-42771800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr19:42766800-42771800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr19:42767000-42769800	Weak transcription	A549	lung
11	chr19:42767800-42771600	Weak transcription	Brain Angular Gyrus	brain
12	chr19:42769800-42770000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr19:42769800-42770200	Enhancers	A549	lung
14	chr19:42770000-42770200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr19:42770000-42770200	Enhancers	Brain Substantia Nigra	brain
16	chr19:42770000-42771600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr19:42770200-42770400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr19:42770200-42770400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr19:42770200-42771400	Weak transcription	A549	lung
20	chr19:42770200-42771800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr19:42770200-42771800	Weak transcription	Brain Substantia Nigra	brain
22	chr19:42770400-42771600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr19:42770400-42771800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr19:42771400-42771600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr19:42771400-42771600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr19:42771400-42771600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr19:42771400-42771600	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr19:42771400-42771600	Weak transcription	Fetal Muscle Trunk	muscle
29	chr19:42771400-42771600	Enhancers	Dnd41	blood
30	chr19:42771400-42771800	Enhancers	Fetal Muscle Leg	muscle
31	chr19:42771400-42771800	Enhancers	A549	lung
32	chr19:42771600-42771800	Enhancers	H9 Cell Line	embryonic stem cell
33	chr19:42771600-42771800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr19:42771600-42771800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr19:42771600-42771800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr19:42771600-42771800	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr19:42771600-42771800	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr19:42771600-42771800	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr19:42771600-42771800	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr19:42771600-42771800	Enhancers	Primary B cells from cord blood	blood
41	chr19:42771600-42771800	Enhancers	Primary T cells from cord blood	blood
42	chr19:42771600-42771800	Enhancers	Primary hematopoietic stem cells	blood
43	chr19:42771600-42771800	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr19:42771600-42771800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr19:42771600-42771800	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr19:42771600-42771800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr19:42771600-42771800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr19:42771600-42771800	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr19:42771600-42771800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr19:42771600-42771800	Enhancers	Primary T helper cells fromperipheralblood	blood

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