Variant report

Variant	rs3764628
Chromosome Location	chr19:18747605-18747606
allele	A/C
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	MAX	chr19:18747570-18748131	A549	lung:	n/a	n/a
2	POLR2A	chr19:18747378-18747651	HCT-116	colon:	n/a	n/a
3	TBP	chr19:18747251-18748067	K562	blood:	n/a	n/a
4	YY1	chr19:18747559-18748169	K562	blood:	n/a	chr19:18747860-18747872 chr19:18747816-18747830
5	MXI1	chr19:18747497-18748188	GM12878	blood:	n/a	n/a
6	SP1	chr19:18746907-18747633	H1-hESC	embryonic stem cell:	n/a	chr19:18747605-18747614 chr19:18747081-18747091 chr19:18747458-18747467 chr19:18747080-18747092 chr19:18747391-18747400 chr19:18747459-18747468 chr19:18747199-18747211 chr19:18747389-18747401 chr19:18747080-18747092 chr19:18747101-18747113 chr19:18747200-18747209 chr19:18747044-18747053 chr19:18747043-18747052 chr19:18747370-18747382 chr19:18747081-18747095 chr19:18747457-18747469 chr19:18747043-18747053 chr19:18747370-18747382 chr19:18747389-18747401 chr19:18747042-18747054 chr19:18747081-18747091 chr19:18747320-18747330 chr19:18747043-18747057 chr19:18747082-18747091 chr19:18747390-18747399 chr19:18747371-18747380 chr19:18747102-18747111 chr19:18747161-18747170 chr19:18747458-18747468 chr19:18747043-18747053 chr19:18747103-18747112 chr19:18747081-18747090 chr19:18747042-18747054 chr19:18747101-18747113 chr19:18747390-18747404 chr19:18747102-18747116 chr19:18747458-18747467 chr19:18747320-18747330 chr19:18747457-18747469 chr19:18747199-18747211 chr19:18747043-18747052
7	CTCF	chr19:18747302-18747605	H1-hESC	embryonic stem cell:	n/a	n/a
8	YY1	chr19:18747560-18748200	HepG2	liver:	n/a	chr19:18747860-18747872 chr19:18747816-18747830
9	HMGN3	chr19:18747335-18748066	K562	blood:	n/a	n/a
10	SPI1	chr19:18747451-18747625	K562	blood:	n/a	n/a
11	RUNX3	chr19:18747094-18747636	GM12878	blood:	n/a	n/a
12	STAT3	chr19:18747588-18747677	MCF10A-Er-Src	breast:	n/a	n/a
13	HCFC1	chr19:18747322-18748050	K562	blood:	n/a	n/a
14	TAF1	chr19:18747304-18748146	H1-neurons	neurons:	n/a	n/a
15	POLR2A	chr19:18747605-18748052	U87	brain:	n/a	n/a
16	MAX	chr19:18747552-18748061	K562	blood:	n/a	n/a
17	SP1	chr19:18747055-18747918	A549	lung:	n/a	chr19:18747761-18747770 chr19:18747605-18747614 chr19:18747081-18747091 chr19:18747458-18747467 chr19:18747080-18747092 chr19:18747391-18747400 chr19:18747760-18747769 chr19:18747459-18747468 chr19:18747709-18747719 chr19:18747199-18747211 chr19:18747389-18747401 chr19:18747080-18747092 chr19:18747101-18747113 chr19:18747200-18747209 chr19:18747635-18747647 chr19:18747370-18747382 chr19:18747081-18747095 chr19:18747457-18747469 chr19:18747370-18747382 chr19:18747389-18747401 chr19:18747760-18747770 chr19:18747760-18747769 chr19:18747081-18747091 chr19:18747320-18747330 chr19:18747082-18747091 chr19:18747390-18747399 chr19:18747371-18747380 chr19:18747102-18747111 chr19:18747161-18747170 chr19:18747458-18747468 chr19:18747103-18747112 chr19:18747759-18747771 chr19:18747081-18747090 chr19:18747760-18747774 chr19:18747636-18747645 chr19:18747709-18747718 chr19:18747759-18747771 chr19:18747101-18747113 chr19:18747760-18747770 chr19:18747390-18747404 chr19:18747635-18747647 chr19:18747709-18747719 chr19:18747102-18747116 chr19:18747668-18747680 chr19:18747458-18747467 chr19:18747320-18747330 chr19:18747457-18747469 chr19:18747729-18747738 chr19:18747199-18747211 chr19:18747687-18747696
18	TEAD4	chr19:18746933-18747620	ECC-1	luminal epithelium:	n/a	n/a
19	CREB1	chr19:18747530-18748171	K562	blood:	n/a	n/a
20	SP4	chr19:18746926-18747803	H1-hESC	embryonic stem cell:	n/a	chr19:18747197-18747213 chr19:18747099-18747115 chr19:18747706-18747722 chr19:18747757-18747773 chr19:18747455-18747471 chr19:18747368-18747384 chr19:18747040-18747056 chr19:18747101-18747117 chr19:18746963-18746979
21	REST	chr19:18746867-18748358	H1-neurons	neurons:	n/a	n/a
22	IRF1	chr19:18746838-18747894	K562	blood:	n/a	chr19:18747368-18747382 chr19:18747099-18747113 chr19:18747757-18747771 chr19:18747582-18747596 chr19:18746931-18746940 chr19:18747197-18747211 chr19:18747633-18747647 chr19:18747387-18747401 chr19:18747078-18747092 chr19:18747040-18747054
23	MAX	chr19:18747524-18747998	K562	blood:	n/a	n/a
24	CHD2	chr19:18746902-18747891	Hela-S3	cervix:	n/a	n/a
25	CREB1	chr19:18747509-18747978	A549	lung:	n/a	n/a
26	MAX	chr19:18747332-18748080	ECC-1	luminal epithelium:	n/a	n/a
27	MAZ	chr19:18746961-18748377	IMR90	lung:	n/a	n/a
28	TBP	chr19:18747597-18748029	H1-hESC	embryonic stem cell:	n/a	n/a
29	NRF1	chr19:18747318-18748020	GM12878	blood:	n/a	chr19:18747954-18747963 chr19:18747820-18747829
30	STAT1	chr19:18747124-18748000	GM12878	blood:	n/a	n/a
31	SPI1	chr19:18747404-18747648	GM12878	blood:	n/a	n/a
32	MAX	chr19:18746761-18748025	MCF-7	breast:	n/a	n/a
33	EGR1	chr19:18746935-18747611	K562	blood:	n/a	chr19:18747390-18747400 chr19:18747104-18747117 chr19:18747392-18747405 chr19:18747161-18747171 chr19:18747129-18747142
34	BHLHE40	chr19:18746864-18747605	GM12878	blood:	n/a	chr19:18747037-18747046
35	PRDM1	chr19:18747362-18747615	Hela-S3	cervix:	n/a	n/a
36	FOXP2	chr19:18747232-18747995	PFSK-1	brain:	n/a	n/a
37	POLR2A	chr19:18747460-18748277	PFSK-1	brain:	n/a	n/a
38	RCOR1	chr19:18746965-18747751	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr19:18747593-18748803	K562	blood:	n/a	n/a
40	UBTF	chr19:18747519-18747631	K562	blood:	n/a	n/a
41	SP1	chr19:18747093-18747798	GM12878	blood:	n/a	chr19:18747761-18747770 chr19:18747605-18747614 chr19:18747458-18747467 chr19:18747391-18747400 chr19:18747760-18747769 chr19:18747459-18747468 chr19:18747709-18747719 chr19:18747199-18747211 chr19:18747389-18747401 chr19:18747101-18747113 chr19:18747200-18747209 chr19:18747635-18747647 chr19:18747370-18747382 chr19:18747457-18747469 chr19:18747370-18747382 chr19:18747389-18747401 chr19:18747760-18747770 chr19:18747760-18747769 chr19:18747320-18747330 chr19:18747390-18747399 chr19:18747371-18747380 chr19:18747102-18747111 chr19:18747161-18747170 chr19:18747458-18747468 chr19:18747103-18747112 chr19:18747759-18747771 chr19:18747760-18747774 chr19:18747636-18747645 chr19:18747709-18747718 chr19:18747759-18747771 chr19:18747101-18747113 chr19:18747760-18747770 chr19:18747390-18747404 chr19:18747635-18747647 chr19:18747709-18747719 chr19:18747102-18747116 chr19:18747668-18747680 chr19:18747458-18747467 chr19:18747320-18747330 chr19:18747457-18747469 chr19:18747729-18747738 chr19:18747199-18747211 chr19:18747687-18747696
42	POLR2A	chr19:18747540-18748075	Hela-S3	cervix:	n/a	n/a
43	TCF7L2	chr19:18746802-18747744	HCT-116	colon:	n/a	n/a
44	SP1	chr19:18747110-18747729	K562	blood:	n/a	chr19:18747605-18747614 chr19:18747458-18747467 chr19:18747391-18747400 chr19:18747459-18747468 chr19:18747709-18747719 chr19:18747199-18747211 chr19:18747389-18747401 chr19:18747200-18747209 chr19:18747635-18747647 chr19:18747370-18747382 chr19:18747457-18747469 chr19:18747370-18747382 chr19:18747389-18747401 chr19:18747320-18747330 chr19:18747390-18747399 chr19:18747371-18747380 chr19:18747161-18747170 chr19:18747458-18747468 chr19:18747636-18747645 chr19:18747709-18747718 chr19:18747390-18747404 chr19:18747635-18747647 chr19:18747709-18747719 chr19:18747668-18747680 chr19:18747458-18747467 chr19:18747320-18747330 chr19:18747457-18747469 chr19:18747199-18747211 chr19:18747687-18747696
45	POU2F2	chr19:18747412-18748014	GM12878	blood:	n/a	chr19:18747519-18747531
46	SMC3	chr19:18747272-18747708	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr19:18747083-18748201	H1-neurons	neurons:	n/a	n/a
48	NRF1	chr19:18747110-18748159	SK-N-SH	brain:	n/a	chr19:18747954-18747963 chr19:18747820-18747829
49	SREBP1	chr19:18747360-18747745	HepG2	liver:	n/a	n/a
50	MAZ	chr19:18747021-18747913	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:18746749..18750617-chr19:18752436..18756057,4	K562	blood:
2	chr19:18738729..18743227-chr19:18745299..18749316,6	K562	blood:
3	chr19:18553947..18555891-chr19:18746913..18749059,2	K562	blood:
4	chr19:18703681..18707981-chr19:18746387..18750076,5	K562	blood:
5	chr19:18716807..18719687-chr19:18745756..18748857,3	K562	blood:
6	chr19:18681409..18685264-chr19:18744559..18747664,3	MCF-7	breast:
7	chr19:18747079..18749227-chr19:18751650..18755741,5	MCF-7	breast:
8	chr19:18681104..18684544-chr19:18745683..18749906,4	K562	blood:
9	chr19:18698512..18700358-chr19:18745222..18750244,4	K562	blood:
10	chr19:18698708..18701515-chr19:18746316..18749182,4	MCF-7	breast:
11	chr19:18740493..18743219-chr19:18745834..18748100,2	K562	blood:
12	chr19:18717575..18719687-chr19:18746806..18748857,2	K562	blood:
13	chr19:18744967..18748846-chr19:18753096..18757449,4	MCF-7	breast:
14	chr19:18744815..18748522-chr19:18792822..18794594,3	K562	blood:

Variant related genes	Relation type
KLHL26	TF binding region
RN7SL155P	TF binding region
ENSG00000221983	Chromatin interaction
ENSG00000105696	Chromatin interaction
ENSG00000006015	Chromatin interaction
ENSG00000167487	Chromatin interaction
ENSG00000006016	Chromatin interaction
ENSG00000263490	Chromatin interaction
ENSG00000256989	Chromatin interaction
ENSG00000105662	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10412356	1.00[YRI][hapmap]
rs10424149	0.81[ASN][1000 genomes]
rs11665980	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11667450	0.97[ASN][1000 genomes]
rs11668413	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11670437	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11672177	0.90[ASN][1000 genomes]
rs12972147	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12973480	0.85[CEU][hapmap];1.00[GIH][hapmap]
rs17683569	1.00[CHB][hapmap];0.81[CHD][hapmap]
rs17683623	0.85[CEU][hapmap]
rs2238649	1.00[CHB][hapmap];0.86[CHD][hapmap]
rs35322184	0.93[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs3752217	0.91[CEU][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3752218	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61248595	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66840797	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs66969630	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs68074367	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72997346	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72997355	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs752981	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8107912	1.00[CHB][hapmap];0.81[CHD][hapmap]
rs8108207	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1057795	chr19:18453362-18883844	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
2	nsv543925	chr19:18453362-18883844	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	nsv532615	chr19:18534867-18796031	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
4	nsv911281	chr19:18613917-18758255	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
5	nsv911282	chr19:18624964-18928480	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
6	nsv833776	chr19:18638028-18782264	Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
7	nsv911286	chr19:18652844-18811112	Active TSS Flanking Active TSS Enhancers Strong transcription 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 miRNA target site	50 gene(s)	inside rSNPs	diseases
8	nsv911289	chr19:18700047-18811112	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
9	esv3332947	chr19:18745902-18749700	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
10	esv12495	chr19:18746535-18747892	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
11	nsv578759	chr19:18747006-18747845	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
12	esv1849639	chr19:18747006-18780799	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

Variant related diseases (count:1)

Disease	PMID	Source
Orofacial clefts	22419666	GWAS catalog

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs3764628	CYP4F12	cis	cerebellum	SCAN
rs3764628	TMEM59L	cis	cerebellum	SCAN
rs3764628	TSSK6	cis	parietal	SCAN
rs3764628	CRLF1	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18745600-18747800	Enhancers	Fetal Brain Male	brain
2	chr19:18746200-18749000	Enhancers	Fetal Heart	heart
3	chr19:18746600-18748000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr19:18746600-18748600	Active TSS	iPS-15b Cell Line	embryonic stem cell
5	chr19:18746600-18748800	Active TSS	A549	lung
6	chr19:18746800-18747800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr19:18746800-18747800	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr19:18746800-18748000	Active TSS	Rectal Mucosa Donor 29	rectum
9	chr19:18746800-18748000	Active TSS	Thymus	Thymus
10	chr19:18746800-18748000	Active TSS	HepG2	liver
11	chr19:18746800-18748200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr19:18746800-18748200	Active TSS	Breast Myoepithelial Primary Cells	Breast
13	chr19:18746800-18748200	Active TSS	GM12878-XiMat	blood
14	chr19:18746800-18748600	Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr19:18746800-18748600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr19:18746800-18748600	Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr19:18746800-18748600	Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr19:18746800-18748600	Active TSS	Hela-S3	cervix
19	chr19:18746800-18749000	Active TSS	iPS-20b Cell Line	embryonic stem cell
20	chr19:18747000-18747800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr19:18747000-18748000	Active TSS	Primary neutrophils fromperipheralblood	blood
22	chr19:18747000-18748000	Active TSS	Primary hematopoietic stem cells	blood
23	chr19:18747000-18748200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr19:18747000-18748200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr19:18747000-18748200	Active TSS	Brain Substantia Nigra	brain
26	chr19:18747000-18748200	Active TSS	Fetal Brain Female	brain
27	chr19:18747000-18748600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr19:18747000-18748600	Active TSS	Brain Inferior Temporal Lobe	brain
29	chr19:18747000-18748600	Active TSS	Fetal Kidney	kidney
30	chr19:18747000-18748600	Active TSS	Ovary	ovary
31	chr19:18747200-18747800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr19:18747200-18748000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr19:18747200-18748000	Active TSS	Colonic Mucosa	Colon
34	chr19:18747200-18748000	Active TSS	Duodenum Mucosa	Duodenum
35	chr19:18747200-18748000	Active TSS	HMEC	breast
36	chr19:18747200-18748000	Active TSS	NH-A	brain
37	chr19:18747200-18748200	Active TSS	H1 Cell Line	embryonic stem cell
38	chr19:18747200-18748200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr19:18747200-18748200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
40	chr19:18747200-18748200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr19:18747200-18748200	Active TSS	Primary hematopoietic stem cells short term culture	blood
42	chr19:18747200-18748200	Active TSS	Primary T helper naive cells from peripheral blood	blood
43	chr19:18747200-18748200	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
44	chr19:18747200-18748200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr19:18747200-18748200	Active TSS	Brain Hippocampus Middle	brain
46	chr19:18747200-18748200	Active TSS	Colon Smooth Muscle	Colon
47	chr19:18747200-18748200	Active TSS	Duodenum Smooth Muscle	Duodenum
48	chr19:18747200-18748200	Active TSS	Gastric	stomach
49	chr19:18747200-18748200	Active TSS	Small Intestine	intestine
50	chr19:18747200-18748200	Active TSS	HUVEC	blood vessel

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