Variant report

Variant	rs3746277
Chromosome Location	chr19:36239484-36239485
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:373)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:373 , 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	RELA	chr19:36239049-36239861	GM18951	blood:	n/a	n/a
2	SIN3AK20	chr19:36238845-36240002	MCF-7	breast:	n/a	n/a
3	POLR2A	chr19:36238979-36239747	K562	blood:	n/a	n/a
4	POLR2A	chr19:36239069-36239925	GM12878	blood:	n/a	n/a
5	YY1	chr19:36239012-36239679	ECC-1	luminal epithelium:	n/a	chr19:36239242-36239256
6	SP2	chr19:36239061-36239813	H1-hESC	embryonic stem cell:	n/a	chr19:36239405-36239428 chr19:36239342-36239357
7	ELF1	chr19:36238960-36239786	GM12878	blood:	n/a	chr19:36239324-36239337
8	USF1	chr19:36239068-36239522	A549	lung:	n/a	n/a
9	GABPA	chr19:36238996-36239812	SK-N-SH	brain:	n/a	chr19:36239248-36239262
10	ELF1	chr19:36239081-36239677	SK-N-SH	brain:	n/a	chr19:36239324-36239337
11	PML	chr19:36238849-36239982	GM12878	blood:	n/a	n/a
12	NANOG	chr19:36239134-36239570	H1-hESC	embryonic stem cell:	n/a	chr19:36239221-36239235
13	ETS1	chr19:36238900-36239847	A549	lung:	n/a	chr19:36239287-36239300 chr19:36239186-36239199 chr19:36239288-36239301
14	YY1	chr19:36239073-36239705	SK-N-SH	brain:	n/a	chr19:36239242-36239256
15	TAF1	chr19:36239149-36239676	H1-neurons	neurons:	n/a	n/a
16	ELF1	chr19:36239013-36239672	HepG2	liver:	n/a	chr19:36239324-36239337
17	NFIC	chr19:36239174-36239720	HepG2	liver:	n/a	n/a
18	GABPA	chr19:36239063-36239655	K562	blood:	n/a	chr19:36239248-36239262
19	SP2	chr19:36238999-36239703	HepG2	liver:	n/a	chr19:36239405-36239428 chr19:36239342-36239357
20	FOS	chr19:36239079-36239500	MCF10A-Er-Src	breast:	n/a	n/a
21	POLR2A	chr19:36238925-36240047	MCF10A-Er-Src	breast:	n/a	n/a
22	USF1	chr19:36239024-36239765	A549	lung:	n/a	n/a
23	ELF1	chr19:36239010-36239719	K562	blood:	n/a	chr19:36239324-36239337
24	PBX3	chr19:36239220-36239580	GM12878	blood:	n/a	chr19:36239407-36239427
25	TBP	chr19:36238970-36239658	Hela-S3	cervix:	n/a	n/a
26	POLR2A	chr19:36239023-36239788	GM12878	blood:	n/a	n/a
27	POLR2A	chr19:36239361-36239849	GM12878	blood:	n/a	n/a
28	JUND	chr19:36239019-36239823	A549	lung:	n/a	n/a
29	NFIC	chr19:36238948-36239653	HepG2	liver:	n/a	n/a
30	ZBTB33	chr19:36238869-36239656	A549	lung:	n/a	chr19:36239200-36239215
31	MXI1	chr19:36239031-36239832	HepG2	liver:	n/a	n/a
32	YY1	chr19:36239008-36239705	GM12878	blood:	n/a	chr19:36239242-36239256
33	POLR2A	chr19:36239336-36239812	GM12878	blood:	n/a	n/a
34	ELF1	chr19:36238812-36239939	A549	lung:	n/a	chr19:36239324-36239337
35	SIN3AK20	chr19:36239129-36239732	PFSK-1	brain:	n/a	n/a
36	PBX3	chr19:36238996-36239772	A549	lung:	n/a	chr19:36239407-36239427
37	PBX3	chr19:36238809-36239871	A549	lung:	n/a	chr19:36239407-36239427
38	POLR2A	chr19:36239390-36239629	GM12878	blood:	n/a	n/a
39	YY1	chr19:36239112-36239764	ECC-1	luminal epithelium:	n/a	chr19:36239242-36239256
40	MAZ	chr19:36239078-36239746	K562	blood:	n/a	n/a
41	POLR2A	chr19:36238925-36239752	K562	blood:	n/a	n/a
42	POLR2A	chr19:36238971-36239721	K562	blood:	n/a	n/a
43	CREB1	chr19:36238988-36239941	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr19:36239009-36239727	HCT-116	colon:	n/a	n/a
45	GABPA	chr19:36239126-36239609	GM12878	blood:	n/a	chr19:36239248-36239262
46	SP2	chr19:36239001-36239783	HepG2	liver:	n/a	chr19:36239405-36239428 chr19:36239342-36239357
47	TBP	chr19:36239096-36239714	K562	blood:	n/a	n/a
48	MAX	chr19:36238987-36239851	GM12878	blood:	n/a	n/a
49	GABPA	chr19:36238936-36239856	SK-N-SH	brain:	n/a	chr19:36239248-36239262
50	POLR2A	chr19:36238976-36239824	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:36239455-36239505	AG04450	lung:	fetal
2	chr19:36239455-36239505	HNPCEpiC	eye:	n/a
3	chr19:36239455-36239505	Hepatocyte	liver:	n/a
4	chr19:36239455-36239505	HEK293	kidney:	embryo
5	chr19:36239455-36239505	ECC-1	luminal epithelium:	n/a
6	chr19:36239455-36239505	NHBE	bronchial:	n/a
7	chr19:36239455-36239505	GM12892	blood:	n/a
8	chr19:36239455-36239505	NB4	blood:	n/a
9	chr19:36239455-36239505	RPTEC	kidney:	n/a
10	chr19:36239455-36239505	HL-60	blood:	n/a
11	chr19:36239455-36239505	HCM	heart:	n/a
12	chr19:36239455-36239505	SK-N-SH_RA	brain:	n/a
13	chr19:36239455-36239505	ProgFib	skin:	n/a
14	chr19:36239455-36239505	K562	blood:	n/a
15	chr19:36239455-36239505	NH-A	brain:	n/a
16	chr19:36239455-36239505	AG09319	gingival:	n/a
17	chr19:36239455-36239505	SKMC	muscle:	n/a
18	chr19:36239455-36239505	HAEpiC	amniotic membrane:	n/a
19	chr19:36239455-36239505	HCF	heart:	n/a
20	chr19:36239455-36239505	IMR90	lung:	fetal
21	chr19:36239455-36239505	Hela-S3	cervix:	n/a
22	chr19:36239455-36239505	HPAEpiC	pulmonary alveolar:	n/a
23	chr19:36239455-36239505	T-47D	breast:	n/a
24	chr19:36239455-36239505	LNCaP	prostate:	n/a
25	chr19:36239455-36239505	HRPEpiC	eye:	n/a
26	chr19:36239455-36239505	AG09309	skin:	n/a
27	chr19:36239455-36239505	Jurkat	blood:	n/a
28	chr19:36239455-36239505	HCT-116	colon:	n/a
29	chr19:36239455-36239505	HUVEC	blood vessel:	n/a
30	chr19:36239455-36239505	SK-N-MC	brain:	n/a
31	chr19:36239455-36239505	NHDF-neo	bronchial:	n/a
32	chr19:36239455-36239505	SAEC	small airway:	n/a
33	chr19:36239455-36239505	U87	brain:	n/a
34	chr19:36239455-36239505	PrEC	prostate:	n/a
35	chr19:36239455-36239505	GM12878	blood:	n/a
36	chr19:36239455-36239505	AG10803	skin:	n/a
37	chr19:36239455-36239505	BE2_C	brain:	n/a
38	chr19:36239455-36239505	PANC-1	pancreas:	n/a
39	chr19:36239455-36239505	PFSK-1	brain:	n/a
40	chr19:36239455-36239505	AoSMC	blood vessel:	n/a
41	chr19:36239455-36239505	HRCEpiC	kidney:	n/a
42	chr19:36239455-36239505	GM19239	blood:	n/a
43	chr19:36239455-36239505	GM12891	blood:	n/a
44	chr19:36239455-36239505	SK-N-SH	brain:	n/a
45	chr19:36239455-36239505	HRE	kidney:	n/a
46	chr19:36239455-36239505	CMK	blood:	n/a
47	chr19:36239455-36239505	MCF10A-Er-Src	breast:	n/a
48	chr19:36239455-36239505	H1-hESC	embryonic stem cell:	embryo
49	chr19:36239455-36239505	Caco-2	colon:	n/a
50	chr19:36239455-36239505	HepG2	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:36207379..36214815-chr19:36234227..36241330,25	MCF-7	breast:
2	chr19:36239415..36241356-chr19:36242820..36244877,2	MCF-7	breast:
3	chr19:36239375..36241509-chr19:36425781..36428099,2	MCF-7	breast:
4	chr19:36237682..36239540-chr19:36335176..36337549,2	MCF-7	breast:
5	chr19:36239350..36241235-chr19:36263074..36266129,3	MCF-7	breast:
6	chr19:36239474..36241411-chr19:36265453..36267969,2	K562	blood:
7	chr19:36238866..36244880-chr19:36246037..36252437,21	MCF-7	breast:
8	chr19:36239210..36239818-chr20:3387776..3388665,2	NB4	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LIN37-2	chr19:36239468-36239659	NONHSAT065909

No data

Variant related genes	Relation type
LIN37	TF binding region
U2AF1L4	TF binding region
ENSG00000267120	TF binding region
ENSG00000267439	TF binding region
LIN37	CpG island
ENSG00000267120	CpG island
U2AF1L4	CpG island
ENSG00000267439	CpG island
ENSG00000167595	Chromatin interaction
ENSG00000267439	Chromatin interaction
ENSG00000088854	Chromatin interaction
ENSG00000126243	Chromatin interaction
ENSG00000004776	Chromatin interaction
ENSG00000161270	Chromatin interaction
ENSG00000004777	Chromatin interaction
ENSG00000267796	Chromatin interaction
ENSG00000272333	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10401156	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10402601	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10402837	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11549030	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12459634	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2239947	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2293686	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28656784	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2871921	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs34031911	0.86[AFR][1000 genomes]
rs3761087	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3848662	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3848665	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62112162	0.87[EUR][1000 genomes]
rs7260184	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432045	chr19:35556260-36520760	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	nsv911630	chr19:36149761-36290977	Enhancers Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	69 gene(s)	inside rSNPs	diseases
3	nsv458566	chr19:36156588-36265508	Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
4	nsv579422	chr19:36156588-36265508	Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
5	nsv911631	chr19:36169285-36290977	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
6	nsv911632	chr19:36174176-36288297	Strong transcription Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
7	nsv911633	chr19:36206050-36283847	Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	61 gene(s)	inside rSNPs	diseases
8	nsv911634	chr19:36206050-36290977	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	61 gene(s)	inside rSNPs	diseases
9	nsv543996	chr19:36210269-36265431	Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
10	nsv1057830	chr19:36210269-36279794	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
11	nsv543997	chr19:36210269-36279794	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
12	nsv911635	chr19:36217333-36283847	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
13	nsv515536	chr19:36219525-36240960	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
14	nsv458567	chr19:36221051-36283847	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
15	nsv579423	chr19:36221051-36283847	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs3746277	U2AF1L4	Cis_1M	lymphoblastoid	RTeQTL
rs3746277	U2AF1L4	cis	Muscle Skeletal	GTEx
rs3746277	LIN37	Cis_1M	lymphoblastoid	RTeQTL
rs3746277	U2AF1L4	cis	lung	GTEx
rs3746277	U2AF1L4	cis	Esophagus Muscularis	GTEx
rs3746277	TMEM149	Cis_1M	lymphoblastoid	RTeQTL
rs3746277	U2AF1L4	cis	Whole Blood	GTEx
rs3746277	TMEM149	cis	multi-tissue	Pritchard

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36238600-36240800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr19:36238800-36240000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr19:36238800-36240000	Active TSS	Rectal Mucosa Donor 29	rectum
4	chr19:36238800-36240000	Active TSS	NHLF	lung
5	chr19:36238800-36240000	Active TSS	Osteobl	bone
6	chr19:36238800-36240200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr19:36238800-36240200	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr19:36238800-36240200	Active TSS	HUES64 Cell Line	embryonic stem cell
9	chr19:36238800-36240200	Active TSS	iPS-20b Cell Line	embryonic stem cell
10	chr19:36238800-36240200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr19:36238800-36240200	Active TSS	Psoas Muscle	Psoas
12	chr19:36238800-36240400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr19:36238800-36240400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr19:36238800-36240400	Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr19:36238800-36240400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
16	chr19:36238800-36240400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr19:36238800-36240400	Active TSS	Right Atrium	heart
18	chr19:36239000-36239600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr19:36239000-36239600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr19:36239000-36239600	Active TSS	Colonic Mucosa	Colon
21	chr19:36239000-36240000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr19:36239000-36240000	Active TSS	Right Ventricle	heart
23	chr19:36239000-36240200	Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr19:36239000-36240200	Active TSS	H1 Cell Line	embryonic stem cell
25	chr19:36239000-36240200	Active TSS	H9 Cell Line	embryonic stem cell
26	chr19:36239000-36240200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr19:36239000-36240200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr19:36239000-36240400	Flanking Active TSS	Adipose Nuclei	Adipose
29	chr19:36239000-36240800	Active TSS	HSMM	muscle
30	chr19:36239200-36239600	Active TSS	Breast Myoepithelial Primary Cells	Breast
31	chr19:36239200-36239600	Active TSS	Primary monocytes fromperipheralblood	blood
32	chr19:36239200-36239600	Active TSS	Primary neutrophils fromperipheralblood	blood
33	chr19:36239200-36239600	Active TSS	Primary B cells from cord blood	blood
34	chr19:36239200-36239600	Active TSS	Primary B cells from peripheral blood	blood
35	chr19:36239200-36239600	Active TSS	Primary T cells fromperipheralblood	blood
36	chr19:36239200-36239600	Active TSS	Primary hematopoietic stem cells	blood
37	chr19:36239200-36239600	Active TSS	Primary T helper cells fromperipheralblood	blood
38	chr19:36239200-36239600	Active TSS	Primary T killer naive cells fromperipheralblood	blood
39	chr19:36239200-36239600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr19:36239200-36239600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr19:36239200-36239600	Active TSS	Liver	Liver
42	chr19:36239200-36239600	Active TSS	Duodenum Mucosa	Duodenum
43	chr19:36239200-36239600	Active TSS	Fetal Muscle Trunk	muscle
44	chr19:36239200-36239600	Active TSS	Rectal Smooth Muscle	rectum
45	chr19:36239200-36239600	Active TSS	Skeletal Muscle Female	skeletal muscle
46	chr19:36239200-36239600	Active TSS	Monocytes-CD14+_RO01746	blood
47	chr19:36239200-36239800	Active TSS	Primary T helper cells PMA-I stimulated	--
48	chr19:36239200-36239800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
49	chr19:36239200-36239800	Active TSS	Cortex derived primary cultured neurospheres	brain
50	chr19:36239200-36239800	Active TSS	Fetal Adrenal Gland	Adrenal Gland

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