Variant report

Variant	nsv911414
Chromosome Location	chr19:21355473-21454672
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:696)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:696 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:21380495-21380772	K562	blood:	n/a	n/a
2	ARID3A	chr19:21392842-21393238	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:21385779-21386015	K562	blood:	n/a	n/a
4	ATF1	chr19:21380399-21380892	K562	blood:	n/a	n/a
5	ATF2	chr19:21405239-21405611	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr19:21380345-21380653	K562	blood:	n/a	n/a
7	BACH1	chr19:21377763-21378071	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr19:21369719-21369791	K562	blood:	n/a	n/a
9	BCL11A	chr19:21405281-21405550	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr19:21380546-21381220	K562	blood:	n/a	n/a
11	BHLHE40	chr19:21367203-21367237	K562	blood:	n/a	n/a
12	BHLHE40	chr19:21388606-21388806	GM12878	blood:	n/a	n/a
13	CBX3	chr19:21380349-21380863	K562	blood:	n/a	n/a
14	CBX3	chr19:21412796-21413087	K562	blood:	n/a	n/a
15	CBX3	chr19:21412789-21413093	K562	blood:	n/a	n/a
16	CCNT2	chr19:21380478-21380687	K562	blood:	n/a	n/a
17	CEBPB	chr19:21421511-21421818	A549	lung:	n/a	chr19:21421653-21421664
18	CEBPB	chr19:21385894-21386036	K562	blood:	n/a	n/a
19	CEBPB	chr19:21385728-21386076	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr19:21394177-21394275	A549	lung:	n/a	chr19:21394220-21394233
21	CEBPB	chr19:21384620-21384767	HepG2	liver:	n/a	chr19:21384674-21384685
22	CEBPB	chr19:21412935-21412982	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr19:21380299-21380955	K562	blood:	n/a	n/a
24	CEBPB	chr19:21380454-21380736	K562	blood:	n/a	n/a
25	CEBPB	chr19:21386069-21386092	HepG2	liver:	n/a	n/a
26	CEBPB	chr19:21421623-21421728	K562	blood:	n/a	chr19:21421653-21421664
27	CEBPB	chr19:21380391-21380816	K562	blood:	n/a	n/a
28	CEBPB	chr19:21421599-21421797	HepG2	liver:	n/a	chr19:21421653-21421664
29	CEBPD	chr19:21380395-21380862	K562	blood:	n/a	n/a
30	CEBPD	chr19:21380343-21380896	K562	blood:	n/a	n/a
31	CHD2	chr19:21385758-21385985	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr19:21405273-21405553	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr19:21366691-21366810	K562	blood:	n/a	n/a
34	CTCF	chr19:21386100-21386250	GM12864	blood:	n/a	n/a
35	CTCF	chr19:21439626-21439792	GM12878	blood:	n/a	n/a
36	CTCF	chr19:21385780-21385930	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr19:21439409-21439983	A549	lung:	n/a	n/a
38	CTCF	chr19:21385800-21385950	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr19:21439700-21439850	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr19:21385780-21385930	GM12865	blood:	n/a	n/a
41	CTCF	chr19:21385740-21385890	GM12875	blood:	n/a	n/a
42	CTCF	chr19:21385800-21385950	HCFaa	heart:	n/a	n/a
43	CTCF	chr19:21439680-21439830	BE2_C	brain:	n/a	n/a
44	CTCF	chr19:21439680-21439830	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr19:21385820-21385970	HMEC	breast:	n/a	n/a
46	CTCF	chr19:21385754-21385995	LNCaP	prostate:	n/a	n/a
47	CTCF	chr19:21385860-21386010	WI-38	lung:	n/a	n/a
48	CTCF	chr19:21439620-21439770	AG09319	gingival:	n/a	n/a
49	CTCF	chr19:21439700-21439850	HCT-116	colon:	n/a	n/a
50	CTCF	chr19:21439637-21439770	GM13976	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:21366880-21366930	HCM	heart:	n/a
2	chr19:21366880-21366930	SK-N-SH	brain:	n/a
3	chr19:21366880-21366930	HCPEpiC	choroid plexus:	n/a
4	chr19:21366880-21366930	HPAEpiC	pulmonary alveolar:	n/a
5	chr19:21366880-21366930	ECC-1	luminal epithelium:	n/a
6	chr19:21366880-21366930	NT2-D1	testis:	n/a
7	chr19:21366880-21366930	LNCaP	prostate:	n/a
8	chr19:21366880-21366930	BE2_C	brain:	n/a
9	chr19:21366880-21366930	Caco-2	colon:	n/a
10	chr19:21366880-21366930	SK-N-SH_RA	brain:	n/a
11	chr19:21366880-21366930	K562	blood:	n/a
12	chr19:21366880-21366930	Hepatocyte	liver:	n/a
13	chr19:21366880-21366930	U87	brain:	n/a
14	chr19:21366880-21366930	GM12891	blood:	n/a
15	chr19:21366880-21366930	PANC-1	pancreas:	n/a
16	chr19:21366880-21366930	HMEC	breast:	n/a
17	chr19:21366880-21366930	MCF-7	breast:	n/a
18	chr19:21366880-21366930	NH-A	brain:	n/a
19	chr19:21366880-21366930	HAEpiC	amniotic membrane:	n/a
20	chr19:21366880-21366930	ProgFib	skin:	n/a
21	chr19:21366880-21366930	HRCEpiC	kidney:	n/a
22	chr19:21366880-21366930	AG04450	lung:	fetal
23	chr19:21366880-21366930	Jurkat	blood:	n/a
24	chr19:21366880-21366930	T-47D	breast:	n/a
25	chr19:21366880-21366930	BJ	skin:	n/a
26	chr19:21366880-21366930	PFSK-1	brain:	n/a
27	chr19:21366880-21366930	IMR90	lung:	fetal
28	chr19:21366880-21366930	AoSMC	blood vessel:	n/a
29	chr19:21366880-21366930	AG09309	skin:	n/a
30	chr19:21366880-21366930	GM12892	blood:	n/a
31	chr19:21366880-21366930	CMK	blood:	n/a
32	chr19:21366880-21366930	HRE	kidney:	n/a
33	chr19:21366880-21366930	SAEC	small airway:	n/a
34	chr19:21366880-21366930	SKMC	muscle:	n/a
35	chr19:21366880-21366930	NHDF-neo	bronchial:	n/a
36	chr19:21366880-21366930	AG04449	skin:	fetal
37	chr19:21366880-21366930	HCT-116	colon:	n/a
38	chr19:21366880-21366930	SK-N-MC	brain:	n/a
39	chr19:21366880-21366930	A549	lung:	n/a
40	chr19:21366880-21366930	GM19239	blood:	n/a
41	chr19:21366880-21366930	HUVEC	blood vessel:	n/a
42	chr19:21366880-21366930	AG09319	gingival:	n/a
43	chr19:21366880-21366930	Hela-S3	cervix:	n/a
44	chr19:21366880-21366930	ovcar-3	ovarian:	n/a
45	chr19:21366880-21366930	GM12878	blood:	n/a
46	chr19:21366880-21366930	HepG2	liver:	n/a
47	chr19:21366880-21366930	HCF	heart:	n/a
48	chr19:21366880-21366930	HRPEpiC	eye:	n/a
49	chr19:21366880-21366930	MCF10A-Er-Src	breast:	n/a
50	chr19:21366880-21366930	H1-hESC	embryonic stem cell:	embryo

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

No.	Distal block	Cell Line	Cell type
1	chr19:21366435..21372841-chr19:21372957..21377596,6	K562	blood:
2	chr19:21392274..21393855-chr19:21395475..21398127,2	K562	blood:
3	chr19:21257717..21259573-chr19:21372943..21374798,2	K562	blood:
4	chr19:21392274..21393855-chr19:21395475..21398127,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF708-10	chr19:21404447-21405548	NONHSAT063691
2	lnc-ZNF708-9	chr19:21427315-21427409	NONHSAT063692
3	lnc-ZNF431-2	chr19:21367295-21367400	NONHSAT063688
4	lnc-ZNF708-9	chr19:21427914-21428043	NONHSAT063692
5	lnc-ZNF431-2	chr19:21372668-21373029	NONHSAT063688
6	lnc-ZNF708-9	chr19:21407900-21407987	NONHSAT063692
7	lnc-ZNF431-2	chr19:21368747-21369090	NONHSAT063689
8	lnc-ZNF431-2	chr19:21372668-21372801	NONHSAT063689
9	lnc-ZNF431-1	chr19:21371401-21371756	NONHSAT063690

No data

Variant related genes	Relation type
RPL36AP51	TF binding region
ENSG00000268892	TF binding region
ENSG00000269839	TF binding region
VN1R82P	TF binding region
ZNF431	TF binding region
RPL36AP51	CpG island
ENSG00000268892	CpG island
ENSG00000269839	CpG island
VN1R82P	CpG island
ZNF431	CpG island
ENSG00000196705	chromatin interactions
ENSG00000268995	chromatin interactions

Extended variants
information (count: 4026 )
Associated
traits (count: 44 )

Variant overlapped rSNPs/rCNVs (count:4026 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2115498	chr19:21355473-21355474	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553819184	chr19:21355489-21355490	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs547994782	chr19:21355490-21355491	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs575689051	chr19:21355508-21355509	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs567709740	chr19:21355530-21355531	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs191108031	chr19:21355560-21355561	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs556370561	chr19:21355561-21355562	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs570110344	chr19:21355601-21355602	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs183129530	chr19:21355668-21355669	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs149290031	chr19:21355692-21355693	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs572385487	chr19:21355693-21355694	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs34524942	chr19:21355787-21355788	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs540939823	chr19:21355798-21355799	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs554758994	chr19:21355821-21355822	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs185779954	chr19:21355846-21355847	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs574537267	chr19:21355902-21355903	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs73541751	chr19:21355956-21355957	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs76731094	chr19:21355958-21355959	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs146253722	chr19:21355978-21355979	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs576467103	chr19:21356001-21356002	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs533316642	chr19:21356052-21356053	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs545411893	chr19:21356088-21356089	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs59345830	chr19:21356115-21356116	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs397978451	chr19:21356117-21356118	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs558897663	chr19:21356139-21356140	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs10419810	chr19:21356215-21356216	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs370986074	chr19:21356262-21356263	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs139191057	chr19:21356280-21356281	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs568801534	chr19:21356281-21356282	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs528892596	chr19:21356313-21356314	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs561566193	chr19:21356318-21356319	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs530226056	chr19:21356319-21356320	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs570049013	chr19:21356324-21356325	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs368396677	chr19:21356395-21356396	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs57941450	chr19:21356414-21356415	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs376873489	chr19:21356453-21356454	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs552625523	chr19:21356477-21356478	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs190453042	chr19:21356572-21356573	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs144069326	chr19:21356573-21356574	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs576333172	chr19:21356599-21356600	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs554565546	chr19:21356610-21356611	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs183180309	chr19:21356641-21356642	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs375554491	chr19:21356688-21356689	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs187883121	chr19:21356699-21356700	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs543372901	chr19:21356702-21356703	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs145970811	chr19:21356751-21356752	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs556705047	chr19:21356770-21356771	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs368237792	chr19:21356805-21356806	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs193282705	chr19:21356813-21356814	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs537927570	chr19:21356820-21356821	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:44)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	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
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:902 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21325400-21361800	Weak transcription	Small Intestine	intestine
2	chr19:21325600-21365800	Weak transcription	Brain Angular Gyrus	brain
3	chr19:21326000-21361000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr19:21326800-21361800	Weak transcription	Stomach Mucosa	stomach
5	chr19:21331000-21371000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr19:21332800-21356400	Weak transcription	Rectal Smooth Muscle	rectum
7	chr19:21333000-21373000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr19:21333200-21357400	Weak transcription	Pancreas	Pancrea
9	chr19:21333400-21364800	Weak transcription	HUVEC	blood vessel
10	chr19:21334600-21360800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr19:21335000-21365000	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr19:21335800-21357000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr19:21335800-21362800	Weak transcription	Psoas Muscle	Psoas
14	chr19:21336000-21357800	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr19:21336000-21362000	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr19:21336200-21361800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr19:21336200-21361800	Weak transcription	Stomach Smooth Muscle	stomach
18	chr19:21336600-21360600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr19:21337000-21357000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr19:21339400-21361000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr19:21339400-21361000	Weak transcription	NHDF-Ad	bronchial
22	chr19:21341800-21361600	Weak transcription	Colon Smooth Muscle	Colon
23	chr19:21342800-21356800	Strong transcription	Dnd41	blood
24	chr19:21342800-21362600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
25	chr19:21343400-21358600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr19:21343600-21359800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr19:21343800-21356400	Weak transcription	Aorta	Aorta
28	chr19:21344200-21359000	Strong transcription	Primary B cells from cord blood	blood
29	chr19:21345400-21356400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr19:21345400-21357800	Weak transcription	Fetal Brain Male	brain
31	chr19:21345400-21358600	Weak transcription	Colonic Mucosa	Colon
32	chr19:21345400-21359200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr19:21345400-21361400	Weak transcription	Spleen	Spleen
34	chr19:21345600-21363000	Weak transcription	HepG2	liver
35	chr19:21347200-21357800	Weak transcription	Gastric	stomach
36	chr19:21348400-21359200	Strong transcription	HUES48 Cell Line	embryonic stem cell
37	chr19:21348600-21356600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr19:21348600-21359200	Strong transcription	HUES64 Cell Line	embryonic stem cell
39	chr19:21348600-21359800	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr19:21348600-21366400	Weak transcription	Brain Substantia Nigra	brain
41	chr19:21349000-21359000	Strong transcription	HUES6 Cell Line	embryonic stem cell
42	chr19:21349400-21356800	Strong transcription	Primary neutrophils fromperipheralblood	blood
43	chr19:21349400-21358800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr19:21349400-21359800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr19:21349600-21358000	Strong transcription	Fetal Stomach	stomach
46	chr19:21349600-21359800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr19:21349600-21370600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr19:21349800-21358400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr19:21349800-21360000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr19:21349800-21360200	Strong transcription	Duodenum Mucosa	Duodenum

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