Variant report

Variant	rs1550477
Chromosome Location	chr16:30773822-30773823
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:293)
CpG islands
(count:0)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	YY1	chr16:30773373-30773853	K562	blood:	n/a	chr16:30773644-30773661 chr16:30773578-30773592
2	POLR2A	chr16:30773479-30773881	GM12878	blood:	n/a	n/a
3	POLR2A	chr16:30773531-30773831	H1-hESC	embryonic stem cell:	n/a	n/a
4	POLR2A	chr16:30772591-30774779	H1-hESC	embryonic stem cell:	n/a	n/a
5	CREB1	chr16:30773298-30773862	ECC-1	luminal epithelium:	n/a	n/a
6	POLR2A	chr16:30773457-30773911	GM12891	blood:	n/a	n/a
7	CTCF	chr16:30773680-30773830	GM12878	blood:	n/a	chr16:30773713-30773721
8	YY1	chr16:30773759-30773891	K562	blood:	n/a	n/a
9	POLR2A	chr16:30773505-30773862	A549	lung:	n/a	n/a
10	TCF12	chr16:30773044-30774034	ECC-1	luminal epithelium:	n/a	n/a
11	CTCF	chr16:30773720-30773870	GM12873	blood:	n/a	n/a
12	POLR2A	chr16:30773506-30773902	HepG2	liver:	n/a	n/a
13	TAF1	chr16:30773209-30774046	H1-hESC	embryonic stem cell:	n/a	n/a
14	TBP	chr16:30773298-30773898	K562	blood:	n/a	n/a
15	SIN3AK20	chr16:30773121-30773829	HepG2	liver:	n/a	n/a
16	POLR2A	chr16:30773153-30773873	HCT-116	colon:	n/a	n/a
17	MAX	chr16:30772771-30773874	K562	blood:	n/a	n/a
18	REST	chr16:30773413-30773869	HepG2	liver:	n/a	n/a
19	SIN3AK20	chr16:30773076-30773903	A549	lung:	n/a	n/a
20	MXI1	chr16:30772591-30774057	HepG2	liver:	n/a	chr16:30773431-30773446
21	HA-E2F1	chr16:30772657-30773839	MCF-7	breast:	n/a	chr16:30772851-30772863 chr16:30773572-30773579 chr16:30773452-30773461 chr16:30773576-30773585
22	TCF7L2	chr16:30773441-30774048	HCT-116	colon:	n/a	n/a
23	MAX	chr16:30773269-30773822	K562	blood:	n/a	n/a
24	POLR2A	chr16:30773470-30773889	A549	lung:	n/a	n/a
25	YY1	chr16:30773442-30774031	NT2-D1	testis:	n/a	chr16:30773644-30773661 chr16:30773578-30773592
26	POLR2A	chr16:30773347-30774005	GM12892	blood:	n/a	n/a
27	POLR2A	chr16:30772296-30774034	ECC-1	luminal epithelium:	n/a	n/a
28	POLR2A	chr16:30772531-30773938	PFSK-1	brain:	n/a	n/a
29	REST	chr16:30772725-30774552	H1-neurons	neurons:	n/a	chr16:30773391-30773400
30	SIN3AK20	chr16:30772534-30773949	PANC-1	pancreas:	n/a	n/a
31	POLR2A	chr16:30772941-30773978	PANC-1	pancreas:	n/a	n/a
32	RELA	chr16:30773362-30773910	GM19099	blood:	n/a	n/a
33	TCF7L2	chr16:30773562-30774052	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr16:30773061-30773959	HUVEC	blood vessel:	n/a	n/a
35	MTA3	chr16:30772071-30774221	GM12878	blood:	n/a	n/a
36	NFIC	chr16:30773072-30773909	ECC-1	luminal epithelium:	n/a	n/a
37	MYBL2	chr16:30773292-30774072	HepG2	liver:	n/a	n/a
38	POLR2A	chr16:30773351-30773889	GM12891	blood:	n/a	n/a
39	SIN3AK20	chr16:30772536-30773977	SK-N-SH	brain:	n/a	n/a
40	ZBTB7A	chr16:30773705-30773920	HepG2	liver:	n/a	n/a
41	POLR2A	chr16:30772707-30773958	Gliobla	brain:	n/a	n/a
42	POLR2A	chr16:30773200-30773870	MCF10A-Er-Src	breast:	n/a	n/a
43	ZBTB7A	chr16:30773533-30773993	K562	blood:	n/a	n/a
44	MXI1	chr16:30773091-30773886	K562	blood:	n/a	chr16:30773431-30773446
45	CTCF	chr16:30773700-30773850	SAEC	small airway:	n/a	chr16:30773713-30773721
46	TAF1	chr16:30772972-30774100	ECC-1	luminal epithelium:	n/a	n/a
47	POLR2A	chr16:30773169-30773890	HCT-116	colon:	n/a	n/a
48	POLR2A	chr16:30773124-30773905	K562	blood:	n/a	n/a
49	TCF3	chr16:30773516-30773911	GM12878	blood:	n/a	chr16:30773713-30773727 chr16:30773715-30773724
50	POLR2A	chr16:30772632-30773985	MCF-7	breast:	n/a	n/a

No data

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:30771826..30774840-chr16:30967351..30969175,3	K562	blood:
2	chr16:30749695..30756203-chr16:30770648..30776596,12	K562	blood:
3	chr16:30676794..30679147-chr16:30771507..30774609,3	MCF-7	breast:
4	chr16:30773356..30774086-chr6:27860729..27861422,2	Hela-S3	cervix:
5	chr16:30749130..30756602-chr16:30770748..30777685,19	MCF-7	breast:
6	chr16:30772557..30775902-chr16:30885131..30888267,4	MCF-7	breast:
7	chr16:30661768..30663590-chr16:30773613..30775423,2	MCF-7	breast:
8	chr16:30773605..30774575-chr19:18111762..18112520,2	Hela-S3	cervix:
9	chr16:30771138..30775135-chr16:30932116..30935546,5	K562	blood:
10	chr16:30709959..30711642-chr16:30773675..30775818,2	K562	blood:
11	chr16:30707976..30709572-chr16:30772183..30773840,2	K562	blood:
12	chr16:30712607..30714306-chr16:30771326..30773925,2	K562	blood:
13	chr16:30197720..30200168-chr16:30772376..30774510,2	MCF-7	breast:
14	chr16:30773318..30774039-chr2:74648382..74649344,2	Hela-S3	cervix:
15	chr16:30708426..30712348-chr16:30772033..30775384,7	MCF-7	breast:
16	chr16:30773358..30775666-chr16:30933218..30935538,2	MCF-7	breast:
17	chr1:27481147..27482051-chr16:30773410..30774074,2	HCT-116	colon:

No data

Variant related genes	Relation type
C16orf93	TF binding region
RNF40	TF binding region
ENSG00000233224	Chromatin interaction
ENSG00000197153	Chromatin interaction
ENSG00000105643	Chromatin interaction
ENSG00000260852	Chromatin interaction
ENSG00000260083	Chromatin interaction
ENSG00000159239	Chromatin interaction
ENSG00000260899	Chromatin interaction
ENSG00000156860	Chromatin interaction
ENSG00000005448	Chromatin interaction
ENSG00000090020	Chromatin interaction
ENSG00000261840	Chromatin interaction
ENSG00000196331	Chromatin interaction
ENSG00000099381	Chromatin interaction
ENSG00000099364	Chromatin interaction
ENSG00000080603	Chromatin interaction
ENSG00000102879	Chromatin interaction
ENSG00000265991	Chromatin interaction
ENSG00000222287	Chromatin interaction
ENSG00000156858	Chromatin interaction

Extended variants
information (count: 92 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs10782000	0.88[YRI][hapmap];1.00[AMR][1000 genomes]
rs11150594	1.00[AMR][1000 genomes]
rs11150595	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.94[YRI][hapmap]
rs11648654	1.00[AMR][1000 genomes]
rs12596375	1.00[ASW][hapmap];1.00[LWK][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12596394	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12598056	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12931844	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12933849	1.00[AMR][1000 genomes]
rs1530203	1.00[ASW][hapmap];0.80[MKK][hapmap]
rs2053426	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2099754	1.00[ASW][hapmap];0.95[LWK][hapmap];1.00[MKK][hapmap];0.94[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2099755	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.94[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2919427	0.89[ASW][hapmap]
rs2919429	0.87[ASW][hapmap]
rs2919430	1.00[AMR][1000 genomes]
rs2919431	0.94[YRI][hapmap];1.00[AMR][1000 genomes]
rs2919432	0.88[YRI][hapmap];1.00[AMR][1000 genomes]
rs2919433	1.00[AMR][1000 genomes]
rs2972804	1.00[AMR][1000 genomes]
rs2972809	0.81[YRI][hapmap]
rs2972815	1.00[AMR][1000 genomes]
rs4268760	0.81[AFR][1000 genomes]
rs4617878	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.88[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4889488	1.00[AMR][1000 genomes]
rs4889494	1.00[AMR][1000 genomes]
rs4889500	0.87[ASW][hapmap];0.92[MKK][hapmap];0.94[YRI][hapmap];1.00[AMR][1000 genomes]
rs4889501	1.00[AMR][1000 genomes]
rs4889503	0.88[YRI][hapmap];1.00[AMR][1000 genomes]
rs4889504	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.94[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4889505	0.88[YRI][hapmap];1.00[AMR][1000 genomes]
rs4889507	0.88[AFR][1000 genomes]
rs4889508	0.82[YRI][hapmap];1.00[AMR][1000 genomes]
rs4889509	1.00[ASW][hapmap];0.90[LWK][hapmap];0.80[MKK][hapmap];0.94[YRI][hapmap]
rs4889510	1.00[AMR][1000 genomes]
rs4889528	1.00[AMR][1000 genomes]
rs55635617	1.00[AMR][1000 genomes]
rs56038936	1.00[AMR][1000 genomes]
rs56209507	1.00[AMR][1000 genomes]
rs57225118	1.00[AMR][1000 genomes]
rs57643871	1.00[AMR][1000 genomes]
rs57877247	1.00[AMR][1000 genomes]
rs6565203	1.00[AMR][1000 genomes]
rs6565204	1.00[AMR][1000 genomes]
rs6565205	1.00[AMR][1000 genomes]
rs6565208	0.87[ASW][hapmap];1.00[AMR][1000 genomes]
rs6565209	1.00[AMR][1000 genomes]
rs6565210	1.00[AMR][1000 genomes]
rs71380412	0.81[AFR][1000 genomes]
rs7185136	0.87[ASW][hapmap];0.92[MKK][hapmap];0.94[YRI][hapmap];1.00[AMR][1000 genomes]
rs7188077	0.89[ASW][hapmap];1.00[LWK][hapmap];0.93[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7193412	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7194763	1.00[AMR][1000 genomes]
rs7195583	0.87[ASW][hapmap];0.92[MKK][hapmap];0.94[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7195612	1.00[AMR][1000 genomes]
rs73524581	1.00[AMR][1000 genomes]
rs73524584	1.00[AMR][1000 genomes]
rs73536457	1.00[AMR][1000 genomes]
rs73536466	1.00[AMR][1000 genomes]
rs73536474	1.00[AMR][1000 genomes]
rs73536488	1.00[AMR][1000 genomes]
rs73536498	1.00[AMR][1000 genomes]
rs73536499	1.00[AMR][1000 genomes]
rs8045484	1.00[ASW][hapmap];0.95[LWK][hapmap];0.93[MKK][hapmap];1.00[YRI][hapmap]
rs8045550	1.00[AMR][1000 genomes]
rs8045624	1.00[ASW][hapmap];0.95[LWK][hapmap];0.93[MKK][hapmap];0.94[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8046609	1.00[AMR][1000 genomes]
rs8047743	1.00[AMR][1000 genomes]
rs8048656	0.88[YRI][hapmap];1.00[AMR][1000 genomes]
rs8049589	1.00[AMR][1000 genomes]
rs8050578	0.88[YRI][hapmap];1.00[AMR][1000 genomes]
rs8056105	0.96[AFR][1000 genomes]
rs8058475	1.00[AMR][1000 genomes]
rs893926	0.88[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs893927	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.94[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9319586	0.87[AFR][1000 genomes]
rs9921630	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.94[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9926855	0.91[AFR][1000 genomes]
rs9934046	1.00[AMR][1000 genomes]
rs9941201	0.94[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9941300	0.87[ASW][hapmap];0.92[MKK][hapmap];0.94[YRI][hapmap];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062456	chr16:30442166-31253997	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers 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 miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
2	nsv542898	chr16:30442166-31253997	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
3	nsv469724	chr16:30632445-30840263	Strong transcription Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	143 gene(s)	inside rSNPs	diseases
4	nsv482704	chr16:30632445-30840263	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	143 gene(s)	inside rSNPs	diseases
5	nsv833188	chr16:30632446-30840263	Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	143 gene(s)	inside rSNPs	diseases
6	nsv1064134	chr16:30640293-31087327	Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	238 gene(s)	inside rSNPs	diseases
7	nsv905728	chr16:30642867-30928970	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	171 gene(s)	inside rSNPs	diseases
8	nsv905729	chr16:30642867-31247924	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	387 gene(s)	inside rSNPs	diseases
9	esv1825223	chr16:30669091-30971810	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
10	nsv431451	chr16:30682399-31340999	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	350 gene(s)	inside rSNPs	diseases
11	nsv9438	chr16:30770203-30799442	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:30771600-30776600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr16:30771800-30774600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr16:30771800-30774600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr16:30772200-30774200	Active TSS	ES-I3 Cell Line	embryonic stem cell
5	chr16:30772200-30774200	Active TSS	Fetal Kidney	kidney
6	chr16:30772200-30774600	Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr16:30772200-30774600	Active TSS	iPS-18 Cell Line	embryonic stem cell
8	chr16:30772200-30774800	Active TSS	iPS-15b Cell Line	embryonic stem cell
9	chr16:30772400-30774000	Active TSS	Brain Anterior Caudate	brain
10	chr16:30772400-30774000	Active TSS	Rectal Smooth Muscle	rectum
11	chr16:30772400-30774200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr16:30772400-30774200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr16:30772400-30774200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr16:30772400-30774200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr16:30772400-30774200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr16:30772400-30774200	Active TSS	Colon Smooth Muscle	Colon
17	chr16:30772400-30774200	Active TSS	Pancreatic Islets	Pancreatic Islet
18	chr16:30772400-30774200	Active TSS	Psoas Muscle	Psoas
19	chr16:30772400-30774200	Active TSS	K562	blood
20	chr16:30772400-30774400	Active TSS	HUES64 Cell Line	embryonic stem cell
21	chr16:30772400-30774600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr16:30772400-30774600	Active TSS	H9 Cell Line	embryonic stem cell
23	chr16:30772400-30774600	Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr16:30772600-30774000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr16:30772600-30774000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr16:30772600-30774000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr16:30772600-30774000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr16:30772600-30774000	Active TSS	Primary T killer memory cells from peripheral blood	blood
29	chr16:30772600-30774000	Active TSS	Cortex derived primary cultured neurospheres	brain
30	chr16:30772600-30774000	Active TSS	Brain Cingulate Gyrus	brain
31	chr16:30772600-30774000	Active TSS	Duodenum Smooth Muscle	Duodenum
32	chr16:30772600-30774000	Active TSS	Thymus	Thymus
33	chr16:30772600-30774000	Active TSS	HUVEC	blood vessel
34	chr16:30772600-30774200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
35	chr16:30772600-30774200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr16:30772600-30774200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr16:30772600-30774200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr16:30772600-30774200	Active TSS	Breast Myoepithelial Primary Cells	Breast
39	chr16:30772600-30774200	Active TSS	Muscle Satellite Cultured Cells	--
40	chr16:30772600-30774200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr16:30772600-30774200	Active TSS	Fetal Intestine Large	intestine
42	chr16:30772600-30774200	Active TSS	Sigmoid Colon	Sigmoid Colon
43	chr16:30772600-30774200	Active TSS	GM12878-XiMat	blood
44	chr16:30772600-30774200	Active TSS	NH-A	brain
45	chr16:30772600-30774400	Active TSS	Aorta	Aorta
46	chr16:30772600-30774400	Active TSS	A549	lung
47	chr16:30772600-30774400	Active TSS	NHDF-Ad	bronchial
48	chr16:30772800-30774000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr16:30772800-30774000	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
50	chr16:30772800-30774000	Active TSS	Primary T helper naive cells from peripheral blood	blood

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