Variant report

Variant	nsv2539
Chromosome Location	chr19:53428153-53434560
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:29)
CpG islands
(count:184)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:29 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr19:53428812-53428959	GM12878	blood:	n/a	n/a
2	CTCF	chr19:53432633-53432682	LNCaP	prostate:	n/a	n/a
3	EBF1	chr19:53428795-53428959	GM12878	blood:	n/a	n/a
4	FOS	chr19:53427885-53428432	MCF10A-Er-Src	breast:	n/a	n/a
5	FOS	chr19:53427894-53428341	MCF10A-Er-Src	breast:	n/a	n/a
6	FOS	chr19:53427897-53428393	MCF10A-Er-Src	breast:	n/a	n/a
7	FOS	chr19:53427938-53428291	MCF10A-Er-Src	breast:	n/a	n/a
8	MAFK	chr19:53429101-53429127	K562	blood:	n/a	n/a
9	MYC	chr19:53427924-53428259	MCF10A-Er-Src	breast:	n/a	n/a
10	MYC	chr19:53427706-53428272	MCF10A-Er-Src	breast:	n/a	n/a
11	POLR2A	chr19:53426124-53429666	K562	blood:	n/a	n/a
12	POLR2A	chr19:53431024-53431026	K562	blood:	n/a	n/a
13	POLR2A	chr19:53427983-53428273	GM12878	blood:	n/a	n/a
14	POLR2A	chr19:53428782-53428973	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr19:53429461-53429795	HepG2	liver:	n/a	n/a
16	POLR2A	chr19:53430390-53430639	K562	blood:	n/a	n/a
17	POLR2A	chr19:53428585-53429139	GM12892	blood:	n/a	n/a
18	POLR2A	chr19:53428652-53429129	GM12878	blood:	n/a	n/a
19	POLR2A	chr19:53431739-53432012	K562	blood:	n/a	n/a
20	POLR2A	chr19:53430699-53430795	HepG2	liver:	n/a	n/a
21	POLR2A	chr19:53430387-53430514	GM12878	blood:	n/a	n/a
22	POLR2A	chr19:53429224-53429344	HepG2	liver:	n/a	n/a
23	POLR2A	chr19:53430460-53430652	K562	blood:	n/a	n/a
24	POLR2A	chr19:53428422-53428734	HepG2	liver:	n/a	n/a
25	POLR2A	chr19:53431944-53432019	K562	blood:	n/a	n/a
26	POLR2A	chr19:53430558-53430695	HepG2	liver:	n/a	n/a
27	POLR2A	chr19:53433357-53433542	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr19:53428055-53428292	HepG2	liver:	n/a	n/a
29	STAT3	chr19:53428070-53428206	MCF10A-Er-Src	breast:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53429005-53429055	GM19239	blood:	n/a
2	chr19:53429005-53429055	GM19239	blood:	n/a
3	chr19:53430697-53430747	BJ	skin:	n/a
4	chr19:53432372-53432422	NT2-D1	testis:	n/a
5	chr19:53430697-53430747	NB4	blood:	n/a
6	chr19:53432372-53432422	HepG2	liver:	n/a
7	chr19:53429005-53429055	HRCEpiC	kidney:	n/a
8	chr19:53432372-53432422	SKMC	muscle:	n/a
9	chr19:53429005-53429055	AoSMC	blood vessel:	n/a
10	chr19:53432372-53432422	T-47D	breast:	n/a
11	chr19:53432372-53432422	MCF10A-Er-Src	breast:	n/a
12	chr19:53430697-53430747	HCT-116	colon:	n/a
13	chr19:53430697-53430747	HUVEC	blood vessel:	n/a
14	chr19:53430697-53430747	PFSK-1	brain:	n/a
15	chr19:53432372-53432422	K562	blood:	n/a
16	chr19:53430697-53430747	ProgFib	skin:	n/a
17	chr19:53429005-53429055	GM12892	blood:	n/a
18	chr19:53430697-53430747	SK-N-SH_RA	brain:	n/a
19	chr19:53432372-53432422	U87	brain:	n/a
20	chr19:53430697-53430747	GM19239	blood:	n/a
21	chr19:53430697-53430747	CMK	blood:	n/a
22	chr19:53430697-53430747	HRCEpiC	kidney:	n/a
23	chr19:53432372-53432422	SK-N-MC	brain:	n/a
24	chr19:53432372-53432422	BJ	skin:	n/a
25	chr19:53432372-53432422	GM06990	blood:	n/a
26	chr19:53430697-53430747	HEEpiC	esophagus:	n/a
27	chr19:53432372-53432422	ovcar-3	ovarian:	n/a
28	chr19:53430697-53430747	HepG2	liver:	n/a
29	chr19:53432372-53432422	NHBE	bronchial:	n/a
30	chr19:53430697-53430747	NHDF-neo	bronchial:	n/a
31	chr19:53429005-53429055	A549	lung:	n/a
32	chr19:53430697-53430747	IMR90	lung:	fetal
33	chr19:53432372-53432422	HRCEpiC	kidney:	n/a
34	chr19:53432372-53432422	HIPEpiC	eye:	n/a
35	chr19:53432372-53432422	ProgFib	skin:	n/a
36	chr19:53429005-53429055	LNCaP	prostate:	n/a
37	chr19:53432372-53432422	PANC-1	pancreas:	n/a
38	chr19:53432372-53432422	Hela-S3	cervix:	n/a
39	chr19:53429005-53429055	MCF10A-Er-Src	breast:	n/a
40	chr19:53429005-53429055	NHBE	bronchial:	n/a
41	chr19:53430697-53430747	Caco-2	colon:	n/a
42	chr19:53429005-53429055	HNPCEpiC	eye:	n/a
43	chr19:53429005-53429055	HPAEpiC	pulmonary alveolar:	n/a
44	chr19:53432372-53432422	HEK293	kidney:	embryo
45	chr19:53429005-53429055	BE2_C	brain:	n/a
46	chr19:53430697-53430747	HAEpiC	amniotic membrane:	n/a
47	chr19:53432372-53432422	AG09319	gingival:	n/a
48	chr19:53430697-53430747	Hela-S3	cervix:	n/a
49	chr19:53430697-53430747	HMEC	breast:	n/a
50	chr19:53430697-53430747	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:53425636..53428538-chr19:53430721..53433929,3	K562	blood:
2	chr19:53431907..53434266-chr19:53444043..53446544,2	K562	blood:
3	chr19:53398338..53401958-chr19:53425181..53428572,6	K562	blood:
4	chr19:53424975..53429001-chr19:53430174..53432512,3	K562	blood:
5	chr19:53425636..53428538-chr19:53430721..53433929,3	K562	blood:
6	chr19:53398338..53403121-chr19:53425170..53428184,6	K562	blood:
7	chr19:53424849..53427676-chr19:53433481..53436897,3	K562	blood:
8	chr19:53426133..53428640-chr19:53444456..53447019,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF816-1	chr19:53430388-53432667	NR_037805

No data

Variant related genes	Relation type
ZNF888	TF binding region
ZNF816-ZNF321P	TF binding region
ZNF888	CpG island
ZNF816-ZNF321P	CpG island
ENSG00000180257	chromatin interactions
ENSG00000269646	chromatin interactions
ENSG00000213793	chromatin interactions
ENSG00000182986	chromatin interactions
ENSG00000213801	chromatin interactions

Extended variants
information (count: 319 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:319 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186709901	chr19:53428172-53428173	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs553729459	chr19:53428176-53428177	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs146017536	chr19:53428197-53428198	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs191609995	chr19:53428209-53428210	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs532452380	chr19:53428212-53428213	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs375176528	chr19:53428220-53428221	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs563874756	chr19:53428249-53428250	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs139973388	chr19:53428250-53428251	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs544453111	chr19:53428255-53428256	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs74390103	chr19:53428279-53428280	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs562833173	chr19:53428306-53428307	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs552709256	chr19:53428314-53428315	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs369440790	chr19:53428315-53428316	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs28445194	chr19:53428351-53428352	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs568872463	chr19:53428375-53428376	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs548243967	chr19:53428384-53428385	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs560558222	chr19:53428421-53428422	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs143133977	chr19:53428423-53428424	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs373771002	chr19:53428448-53428449	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs145469464	chr19:53428452-53428453	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs117493343	chr19:53428460-53428461	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs571785767	chr19:53428472-53428473	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs531525671	chr19:53428481-53428482	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs56903618	chr19:53428514-53428515	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs397947301	chr19:53428522-53428523	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs11667788	chr19:53428541-53428542	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs386810610	chr19:53428575-53428576	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs12971956	chr19:53428576-53428577	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs185210001	chr19:53428588-53428589	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs142552559	chr19:53428635-53428636	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs539092296	chr19:53428651-53428652	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs189774045	chr19:53428667-53428668	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs182113824	chr19:53428738-53428739	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs150970236	chr19:53428749-53428750	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs142529439	chr19:53428796-53428797	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs575006107	chr19:53428835-53428836	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs542492345	chr19:53428857-53428858	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs560649515	chr19:53428858-53428859	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs35456478	chr19:53428865-53428866	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs527681927	chr19:53428877-53428878	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs146786764	chr19:53428886-53428887	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs189072086	chr19:53428907-53428908	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs139302187	chr19:53428961-53428962	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs114304653	chr19:53428971-53428972	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs191829748	chr19:53429005-53429006	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs568275878	chr19:53429010-53429011	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs529112881	chr19:53429032-53429033	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs12609561	chr19:53429050-53429051	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs565884491	chr19:53429114-53429115	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs386810611	chr19:53429116-53429117	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	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
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Adrenocortical carcinoma	18281524	CNVD
Melanoma	20877625	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53426600-53444800	Weak transcription	Fetal Heart	heart
2	chr19:53426800-53428200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr19:53426800-53431600	Weak transcription	HSMMtube	muscle
4	chr19:53426800-53432400	Weak transcription	Gastric	stomach
5	chr19:53426800-53434200	Weak transcription	NH-A	brain
6	chr19:53426800-53435600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr19:53426800-53444800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr19:53426800-53445000	Weak transcription	Small Intestine	intestine
9	chr19:53426800-53445200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr19:53426800-53445200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr19:53427000-53428200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr19:53427000-53428200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr19:53427000-53431200	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr19:53427000-53431200	Weak transcription	Pancreas	Pancrea
15	chr19:53427000-53431800	Weak transcription	Esophagus	oesophagus
16	chr19:53427000-53431800	Weak transcription	HSMM	muscle
17	chr19:53427000-53432000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr19:53427000-53433400	Weak transcription	Lung	lung
19	chr19:53427000-53440200	Weak transcription	Aorta	Aorta
20	chr19:53427000-53442600	Weak transcription	Ovary	ovary
21	chr19:53427000-53444800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr19:53427200-53428200	Enhancers	H1 Cell Line	embryonic stem cell
23	chr19:53427200-53428200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr19:53427200-53428200	Enhancers	Primary T cells fromperipheralblood	blood
25	chr19:53427200-53428400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr19:53427200-53428400	Enhancers	NHEK	skin
27	chr19:53427200-53428600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr19:53427200-53429400	Weak transcription	Fetal Intestine Small	intestine
29	chr19:53427200-53430200	Weak transcription	Fetal Stomach	stomach
30	chr19:53427200-53431000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr19:53427200-53431000	Weak transcription	Primary T cells from cord blood	blood
32	chr19:53427200-53431000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr19:53427200-53431200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr19:53427200-53431200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr19:53427200-53431800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr19:53427200-53431800	Weak transcription	Fetal Kidney	kidney
37	chr19:53427200-53431800	Weak transcription	Fetal Thymus	thymus
38	chr19:53427200-53439600	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr19:53427400-53428200	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr19:53427400-53431200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr19:53427400-53431400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr19:53427400-53431600	Weak transcription	Primary T helper cells PMA-I stimulated	--
43	chr19:53427400-53432000	Weak transcription	Brain Cingulate Gyrus	brain
44	chr19:53427400-53444800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr19:53427400-53445000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr19:53427400-53445200	Weak transcription	Left Ventricle	heart
47	chr19:53427600-53428200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr19:53427600-53428200	Enhancers	Placenta	Placenta
49	chr19:53427600-53428200	Enhancers	Rectal Mucosa Donor 29	rectum
50	chr19:53427600-53428400	Enhancers	Primary monocytes fromperipheralblood	blood

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