Variant report

Variant	nsv1062653
Chromosome Location	chr19:40123868-40163241
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:383)
CpG islands
(count:124)
Chromatin interactive
region (count:8)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:383 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr19:40151350-40151658	Hela-S3	cervix:	n/a	chr19:40151501-40151514
2	CEBPB	chr19:40136019-40136106	HepG2	liver:	n/a	chr19:40136071-40136082 chr19:40136071-40136082 chr19:40136072-40136083
3	CEBPB	chr19:40140585-40140785	HepG2	liver:	n/a	chr19:40140634-40140645
4	CHD1	chr19:40162625-40162903	GM12878	blood:	n/a	n/a
5	CTCF	chr19:40162760-40162910	AG09309	skin:	n/a	n/a
6	CTCF	chr19:40162687-40162944	HepG2	liver:	n/a	n/a
7	CTCF	chr19:40162739-40162922	GM20000	blood:	n/a	n/a
8	CTCF	chr19:40162780-40162930	GM12871	blood:	n/a	n/a
9	CTCF	chr19:40162735-40162890	GM12892	blood:	n/a	n/a
10	CTCF	chr19:40163080-40163230	GM12878	blood:	n/a	n/a
11	CTCF	chr19:40162740-40162890	GM06990	blood:	n/a	n/a
12	CTCF	chr19:40163123-40163127	GM10266	blood:	n/a	n/a
13	CTCF	chr19:40162617-40163014	IMR90	lung:	n/a	n/a
14	CTCF	chr19:40163179-40163197	GM12891	blood:	n/a	n/a
15	CTCF	chr19:40162780-40162930	HCT-116	colon:	n/a	n/a
16	CTCF	chr19:40136165-40136226	Fibrobl	skin:	n/a	n/a
17	CTCF	chr19:40162720-40162870	NHDF-neo	bronchial:	n/a	n/a
18	CTCF	chr19:40162720-40162870	HFF	foreskin:	n/a	n/a
19	CTCF	chr19:40162727-40162919	ProgFib	skin:	n/a	n/a
20	CTCF	chr19:40162720-40162870	RPTEC	kidney:	n/a	n/a
21	CTCF	chr19:40162760-40162910	HMF	breast:	n/a	n/a
22	CTCF	chr19:40162711-40162924	NHEK	skin:	n/a	n/a
23	CTCF	chr19:40162760-40162910	HA-sp	spinal cord:	n/a	n/a
24	CTCF	chr19:40162740-40162890	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr19:40162760-40162910	GM12865	blood:	n/a	n/a
26	CTCF	chr19:40163240-40163390	GM12870	blood:	n/a	n/a
27	CTCF	chr19:40162680-40162830	HCT-116	colon:	n/a	n/a
28	CTCF	chr19:40162597-40162995	A549	lung:	n/a	n/a
29	CTCF	chr19:40162682-40162959	Lung_OC	lung:	n/a	n/a
30	CTCF	chr19:40163040-40163290	HMF	breast:	n/a	n/a
31	CTCF	chr19:40162700-40162876	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr19:40162690-40162942	GM12878	blood:	n/a	n/a
33	CTCF	chr19:40162660-40162810	NB4	blood:	n/a	n/a
34	CTCF	chr19:40162649-40162955	GM10248	blood:	n/a	n/a
35	CTCF	chr19:40162740-40162894	GM19238	blood:	n/a	n/a
36	CTCF	chr19:40162715-40162935	LNCaP	prostate:	n/a	n/a
37	CTCF	chr19:40162655-40162924	HepG2	liver:	n/a	n/a
38	CTCF	chr19:40162740-40162890	GM12865	blood:	n/a	n/a
39	CTCF	chr19:40163058-40163156	GM13976	blood:	n/a	n/a
40	CTCF	chr19:40162740-40162890	SAEC	small airway:	n/a	n/a
41	CTCF	chr19:40162712-40162943	LNCaP	prostate:	n/a	n/a
42	CTCF	chr19:40162605-40162896	T-47D	breast:	n/a	n/a
43	CTCF	chr19:40162820-40162970	HAc	cerebellar:	n/a	n/a
44	CTCF	chr19:40162702-40162941	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chr19:40162700-40162850	GM12874	blood:	n/a	n/a
46	CTCF	chr19:40162740-40162890	AG10803	skin:	n/a	n/a
47	CTCF	chr19:40162960-40163110	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr19:40162740-40162890	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr19:40162740-40162890	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr19:40162800-40162950	WI-38	lung:	n/a	n/a

(count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40128901-40128951	SKMC	muscle:	n/a
2	chr19:40128901-40128951	PANC-1	pancreas:	n/a
3	chr19:40128901-40128951	SKMC	muscle:	n/a
4	chr19:40128901-40128951	PANC-1	pancreas:	n/a
5	chr19:40129920-40129970	SAEC	small airway:	n/a
6	chr19:40128901-40128951	NHBE	bronchial:	n/a
7	chr19:40129920-40129970	SK-N-SH_RA	brain:	n/a
8	chr19:40128901-40128951	T-47D	breast:	n/a
9	chr19:40129920-40129970	H1-hESC	embryonic stem cell:	embryo
10	chr19:40129920-40129970	AG04450	lung:	fetal
11	chr19:40128901-40128951	Caco-2	colon:	n/a
12	chr19:40129920-40129970	MCF10A-Er-Src	breast:	n/a
13	chr19:40128901-40128951	ECC-1	luminal epithelium:	n/a
14	chr19:40129920-40129970	T-47D	breast:	n/a
15	chr19:40128901-40128951	Jurkat	blood:	n/a
16	chr19:40129920-40129970	RPTEC	kidney:	n/a
17	chr19:40129920-40129970	ProgFib	skin:	n/a
18	chr19:40128901-40128951	NHDF-neo	bronchial:	n/a
19	chr19:40128901-40128951	HAEpiC	amniotic membrane:	n/a
20	chr19:40128901-40128951	AG09319	gingival:	n/a
21	chr19:40129920-40129970	AG09319	gingival:	n/a
22	chr19:40129920-40129970	BE2_C	brain:	n/a
23	chr19:40129920-40129970	ECC-1	luminal epithelium:	n/a
24	chr19:40129920-40129970	CMK	blood:	n/a
25	chr19:40129920-40129970	GM12878	blood:	n/a
26	chr19:40129920-40129970	ovcar-3	ovarian:	n/a
27	chr19:40128901-40128951	Hepatocyte	liver:	n/a
28	chr19:40129920-40129970	PANC-1	pancreas:	n/a
29	chr19:40128901-40128951	GM12878	blood:	n/a
30	chr19:40129920-40129970	HRPEpiC	eye:	n/a
31	chr19:40129920-40129970	GM12892	blood:	n/a
32	chr19:40129920-40129970	AoSMC	blood vessel:	n/a
33	chr19:40129920-40129970	Caco-2	colon:	n/a
34	chr19:40129920-40129970	HepG2	liver:	n/a
35	chr19:40129920-40129970	Hepatocyte	liver:	n/a
36	chr19:40128901-40128951	HMEC	breast:	n/a
37	chr19:40129920-40129970	HRE	kidney:	n/a
38	chr19:40128901-40128951	HEEpiC	esophagus:	n/a
39	chr19:40129920-40129970	HNPCEpiC	eye:	n/a
40	chr19:40129920-40129970	HMEC	breast:	n/a
41	chr19:40129920-40129970	NHDF-neo	bronchial:	n/a
42	chr19:40128901-40128951	AG04450	lung:	fetal
43	chr19:40128901-40128951	NT2-D1	testis:	n/a
44	chr19:40128901-40128951	MCF-7	breast:	n/a
45	chr19:40128901-40128951	HCF	heart:	n/a
46	chr19:40128901-40128951	AoSMC	blood vessel:	n/a
47	chr19:40128901-40128951	LNCaP	prostate:	n/a
48	chr19:40128901-40128951	BE2_C	brain:	n/a
49	chr19:40128901-40128951	GM06990	blood:	n/a
50	chr19:40128901-40128951	HIPEpiC	eye:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:40041783..40042891-chr19:40162333..40163330,4	K562	blood:
2	chr19:39925057..39927468-chr19:40150682..40153479,2	K562	blood:
3	chr19:39988438..39989161-chr19:40162366..40162932,2	K562	blood:
4	chr19:40041871..40042653-chr19:40162390..40162892,2	MCF-7	breast:
5	chr19:40055301..40057183-chr19:40147250..40149926,2	MCF-7	breast:
6	chr19:40041798..40042719-chr19:40162291..40163385,9	MCF-7	breast:
7	chr19:39988198..39988763-chr19:40162454..40163227,2	MCF-7	breast:
8	chr19:40163210..40165073-chr19:40333318..40334922,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LGALS16-1	chr19:40132792-40133041	NONHSAT066318
2	lnc-LGALS16-1	chr19:40129325-40130608	NONHSAT066318
3	lnc-LGALS16-1	chr19:40131114-40131324	NONHSAT066318
4	lnc-LGALS16-1	chr19:40131461-40131546	NONHSAT066318

No data

Variant related genes	Relation type
LGALS16	TF binding region
ENSG00000268153	TF binding region
ENSG00000269519	TF binding region
ENSG00000268243	TF binding region
LGALS16	CpG island
ENSG00000268153	CpG island
ENSG00000269519	CpG island
ENSG00000268243	CpG island
ENSG00000105193	chromatin interactions
ENSG00000196235	chromatin interactions

Extended variants
information (count: 1432 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1432 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529936246	chr19:40123870-40123871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs71601216	chr19:40123904-40123905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548473042	chr19:40123917-40123918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559150617	chr19:40123928-40123929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs71326274	chr19:40123936-40123937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577514122	chr19:40123938-40123939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2354228	chr19:40123941-40123942	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs553689084	chr19:40123942-40123943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574399421	chr19:40123944-40123945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34488326	chr19:40123946-40123947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562706803	chr19:40123947-40123948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs61945837	chr19:40123948-40123949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs3961728	chr19:40123955-40123956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs79176404	chr19:40123956-40123957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs36186492	chr19:40123957-40123958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541431890	chr19:40123961-40123962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs34028258	chr19:40123962-40123963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs3979234	chr19:40123975-40123976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113177807	chr19:40123979-40123980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35700371	chr19:40123980-40123981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188972906	chr19:40123981-40123982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533804924	chr19:40123989-40123990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575207387	chr19:40123993-40123994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112123782	chr19:40123998-40123999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111982080	chr19:40123999-40124000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563986131	chr19:40124007-40124008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528259700	chr19:40124013-40124014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs3961727	chr19:40124024-40124025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs62337206	chr19:40124040-40124041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75360052	chr19:40124045-40124046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34538260	chr19:40124047-40124048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78515947	chr19:40124048-40124049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs74618421	chr19:40124050-40124051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs74721200	chr19:40124057-40124058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs79203839	chr19:40124060-40124061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs71497057	chr19:40124064-40124065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs28786426	chr19:40124070-40124071	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs4614777	chr19:40124071-40124072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79030574	chr19:40124075-40124076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75136864	chr19:40124080-40124081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4267436	chr19:40124083-40124084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12807222	chr19:40124084-40124085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs71605941	chr19:40124087-40124088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs3979233	chr19:40124090-40124091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs79014301	chr19:40124091-40124092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12802252	chr19:40124092-40124093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs75989076	chr19:40124094-40124095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs72501441	chr19:40124100-40124101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546523192	chr19:40124104-40124105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs80198013	chr19:40124109-40124110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Pleomorphic liposarcoma	18784837	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
Disorders of sex development	21048976	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
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40122000-40127600	Weak transcription	Placenta	Placenta
2	chr19:40127600-40131800	Enhancers	Placenta	Placenta
3	chr19:40128600-40129000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr19:40131800-40132600	Weak transcription	Placenta	Placenta
5	chr19:40131800-40133600	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr19:40132000-40133400	Enhancers	HepG2	liver
7	chr19:40132200-40133000	Bivalent Enhancer	A549	lung
8	chr19:40132600-40133200	Enhancers	Placenta	Placenta
9	chr19:40133200-40151200	Weak transcription	Placenta	Placenta
10	chr19:40146800-40147000	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr19:40147000-40147200	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr19:40148600-40149400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr19:40150600-40151200	Bivalent Enhancer	GM12878-XiMat	blood
14	chr19:40152200-40153000	Enhancers	Primary T cells from cord blood	blood
15	chr19:40161200-40162600	Enhancers	H9 Cell Line	embryonic stem cell
16	chr19:40161200-40162600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr19:40161200-40162600	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr19:40161200-40162600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr19:40161200-40162800	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr19:40161200-40162800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr19:40161200-40162800	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr19:40161200-40162800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr19:40161400-40162600	Enhancers	H1 Cell Line	embryonic stem cell
24	chr19:40161400-40162800	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr19:40161800-40162000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr19:40162400-40162600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr19:40162400-40162600	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
28	chr19:40162400-40162600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr19:40162400-40162600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr19:40162400-40162600	Enhancers	Brain Hippocampus Middle	brain
31	chr19:40162400-40162800	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr19:40162400-40163200	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr19:40162400-40163200	Enhancers	GM12878-XiMat	blood
34	chr19:40162400-40164600	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr19:40162400-40164600	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr19:40162600-40162800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
37	chr19:40162600-40162800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr19:40162600-40163600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr19:40162600-40164200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr19:40162600-40164600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chr19:40162600-40164600	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr19:40162600-40169600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr19:40162800-40163000	Enhancers	Skeletal Muscle Male	skeletal muscle
44	chr19:40162800-40163000	Bivalent Enhancer	A549	lung
45	chr19:40162800-40163800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr19:40162800-40164200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr19:40162800-40164400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr19:40162800-40164600	Enhancers	Primary T helper cells fromperipheralblood	blood
49	chr19:40162800-40166800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr19:40163000-40164200	Enhancers	Primary T cells fromperipheralblood	blood

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