Variant report

Variant	rs193134595
Chromosome Location	chr4:10459160-10459161
allele	A/G
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	E2F6	chr4:10458677-10459161	K562	blood:	n/a	chr4:10458681-10458691 chr4:10459082-10459091 chr4:10459062-10459071 chr4:10459129-10459138 chr4:10458680-10458691
2	POLR2A	chr4:10458208-10459346	GM18505	blood:	n/a	n/a
3	MAX	chr4:10458651-10459185	ECC-1	luminal epithelium:	n/a	chr4:10458720-10458729
4	E2F6	chr4:10458638-10459406	A549	lung:	n/a	chr4:10458681-10458691 chr4:10459082-10459091 chr4:10459309-10459319 chr4:10459062-10459071 chr4:10459129-10459138 chr4:10458680-10458691
5	POLR2A	chr4:10458236-10459340	HUVEC	blood vessel:	n/a	n/a
6	MAX	chr4:10458001-10459464	A549	lung:	n/a	chr4:10458720-10458729
7	UBTF	chr4:10458839-10460197	K562	blood:	n/a	n/a
8	EGR1	chr4:10458974-10459269	K562	blood:	n/a	chr4:10459062-10459071 chr4:10459130-10459143 chr4:10459130-10459140 chr4:10459130-10459143 chr4:10459131-10459140 chr4:10459127-10459141 chr4:10459130-10459143
9	POLR2A	chr4:10458014-10459351	PBDE	blood:	n/a	n/a
10	ZNF143	chr4:10458056-10459249	GM12878	blood:	n/a	chr4:10459124-10459134 chr4:10458628-10458638
11	MYC	chr4:10458993-10459251	K562	blood:	n/a	n/a
12	TAF1	chr4:10458823-10459219	K562	blood:	n/a	n/a
13	POLR2A	chr4:10458919-10459283	GM12878	blood:	n/a	n/a
14	NRF1	chr4:10458876-10459290	H1-hESC	embryonic stem cell:	n/a	chr4:10459079-10459090 chr4:10459044-10459055 chr4:10459061-10459072 chr4:10459061-10459072 chr4:10459061-10459075 chr4:10459058-10459072 chr4:10459063-10459072
15	POLR2A	chr4:10458205-10459299	GM19193	blood:	n/a	n/a
16	POLR2A	chr4:10458221-10459298	GM19099	blood:	n/a	n/a
17	EGR1	chr4:10458901-10459286	K562	blood:	n/a	chr4:10459062-10459071 chr4:10459130-10459143 chr4:10459130-10459140 chr4:10459130-10459143 chr4:10459131-10459140 chr4:10459127-10459141 chr4:10459130-10459143
18	SETDB1	chr4:10458127-10459374	K562	blood:	n/a	chr4:10459062-10459071
19	POLR2A	chr4:10458224-10459166	IMR90	lung:	n/a	n/a
20	ZBTB7A	chr4:10458827-10459179	K562	blood:	n/a	chr4:10458909-10458917
21	POLR2A	chr4:10458835-10459243	HCT-116	colon:	n/a	n/a
22	E2F6	chr4:10458136-10459409	K562	blood:	n/a	chr4:10458681-10458691 chr4:10459082-10459091 chr4:10458501-10458513 chr4:10458501-10458510 chr4:10459309-10459319 chr4:10459062-10459071 chr4:10459129-10459138 chr4:10458680-10458691
23	POLR2A	chr4:10458027-10459413	K562	blood:	n/a	n/a
24	POLR2A	chr4:10458014-10459177	GM12878	blood:	n/a	n/a
25	NANOG	chr4:10458920-10459314	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr4:10458770-10459230	PANC-1	pancreas:	n/a	n/a
27	NRF1	chr4:10458952-10459210	K562	blood:	n/a	chr4:10459079-10459090 chr4:10459044-10459055 chr4:10459061-10459072 chr4:10459061-10459072 chr4:10459061-10459075 chr4:10459058-10459072 chr4:10459063-10459072
28	PML	chr4:10458828-10459309	K562	blood:	n/a	n/a
29	HEY1	chr4:10458831-10459202	K562	blood:	n/a	chr4:10459077-10459092 chr4:10459124-10459139 chr4:10459130-10459145 chr4:10459048-10459063
30	POLR2A	chr4:10458773-10459262	H1-neurons	neurons:	n/a	n/a
31	POLR2A	chr4:10458764-10459238	HCT-116	colon:	n/a	n/a
32	BHLHE40	chr4:10458951-10459247	GM12878	blood:	n/a	chr4:10459125-10459141
33	ZNF143	chr4:10459112-10459180	K562	blood:	n/a	chr4:10459124-10459134
34	HCFC1	chr4:10459023-10459216	K562	blood:	n/a	n/a
35	MAX	chr4:10457933-10460233	K562	blood:	n/a	chr4:10458720-10458729 chr4:10459964-10459974
36	MAX	chr4:10457997-10459307	GM12878	blood:	n/a	chr4:10458720-10458729
37	POLR2A	chr4:10458813-10459212	HUVEC	blood vessel:	n/a	n/a
38	HEY1	chr4:10458865-10459307	K562	blood:	n/a	chr4:10459077-10459092 chr4:10459124-10459139 chr4:10459130-10459145 chr4:10459048-10459063
39	POLR2A	chr4:10458775-10459330	SK-N-MC	brain:	n/a	n/a
40	POLR2A	chr4:10458836-10459296	PANC-1	pancreas:	n/a	n/a
41	ELF1	chr4:10458038-10459429	GM12878	blood:	n/a	chr4:10459128-10459140 chr4:10459042-10459054 chr4:10458442-10458455
42	MAZ	chr4:10458905-10459428	GM12878	blood:	n/a	n/a
43	TBL1XR1	chr4:10458929-10459161	GM12878	blood:	n/a	n/a
44	NRF1	chr4:10458877-10459269	GM12878	blood:	n/a	chr4:10459079-10459090 chr4:10459044-10459055 chr4:10459061-10459072 chr4:10459061-10459072 chr4:10459061-10459075 chr4:10459058-10459072 chr4:10459063-10459072
45	EGR1	chr4:10458949-10459245	GM12878	blood:	n/a	chr4:10459062-10459071 chr4:10459130-10459143 chr4:10459130-10459140 chr4:10459130-10459143 chr4:10459131-10459140 chr4:10459127-10459141 chr4:10459130-10459143
46	MYC	chr4:10458887-10459430	K562	blood:	n/a	n/a
47	ZNF143	chr4:10458872-10459303	H1-hESC	embryonic stem cell:	n/a	chr4:10459124-10459134
48	POLR2A	chr4:10458192-10459320	GM12878	blood:	n/a	n/a
49	POLR2A	chr4:10458686-10459213	HUVEC	blood vessel:	n/a	n/a
50	POLR2A	chr4:10458199-10459318	GM15510	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10459132-10459182	Caco-2	colon:	n/a
2	chr4:10459132-10459182	NB4	blood:	n/a
3	chr4:10459128-10459178	HRCEpiC	kidney:	n/a
4	chr4:10459128-10459178	HCM	heart:	n/a
5	chr4:10459141-10459191	NT2-D1	testis:	n/a
6	chr4:10459132-10459182	HCPEpiC	choroid plexus:	n/a
7	chr4:10459132-10459182	MCF10A-Er-Src	breast:	n/a
8	chr4:10459141-10459191	AG10803	skin:	n/a
9	chr4:10459141-10459191	ECC-1	luminal epithelium:	n/a
10	chr4:10459132-10459182	HUVEC	blood vessel:	n/a
11	chr4:10459132-10459182	LNCaP	prostate:	n/a
12	chr4:10459132-10459182	SK-N-SH_RA	brain:	n/a
13	chr4:10459141-10459191	T-47D	breast:	n/a
14	chr4:10459132-10459182	GM12892	blood:	n/a
15	chr4:10459141-10459191	PrEC	prostate:	n/a
16	chr4:10459141-10459191	ProgFib	skin:	n/a
17	chr4:10459141-10459191	SK-N-SH	brain:	n/a
18	chr4:10459132-10459182	HCM	heart:	n/a
19	chr4:10459132-10459182	GM19239	blood:	n/a
20	chr4:10459132-10459182	HRPEpiC	eye:	n/a
21	chr4:10459141-10459191	AG04449	skin:	fetal
22	chr4:10459128-10459178	GM06990	blood:	n/a
23	chr4:10459132-10459182	PrEC	prostate:	n/a
24	chr4:10459141-10459191	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:10459128-10459178	MCF10A-Er-Src	breast:	n/a
26	chr4:10459128-10459178	Caco-2	colon:	n/a
27	chr4:10459141-10459191	HMEC	breast:	n/a
28	chr4:10459132-10459182	HL-60	blood:	n/a
29	chr4:10459128-10459178	HPAEpiC	pulmonary alveolar:	n/a
30	chr4:10459132-10459182	NT2-D1	testis:	n/a
31	chr4:10459132-10459182	T-47D	breast:	n/a
32	chr4:10459128-10459178	AG09319	gingival:	n/a
33	chr4:10459128-10459178	ECC-1	luminal epithelium:	n/a
34	chr4:10459128-10459178	SKMC	muscle:	n/a
35	chr4:10459141-10459191	SAEC	small airway:	n/a
36	chr4:10459128-10459178	GM12878	blood:	n/a
37	chr4:10459132-10459182	MCF-7	breast:	n/a
38	chr4:10459128-10459178	ovcar-3	ovarian:	n/a
39	chr4:10459141-10459191	HEK293	kidney:	embryo
40	chr4:10459141-10459191	A549	lung:	n/a
41	chr4:10459128-10459178	HMEC	breast:	n/a
42	chr4:10459132-10459182	HCT-116	colon:	n/a
43	chr4:10459132-10459182	BE2_C	brain:	n/a
44	chr4:10459141-10459191	K562	blood:	n/a
45	chr4:10459132-10459182	GM12891	blood:	n/a
46	chr4:10459128-10459178	HCPEpiC	choroid plexus:	n/a
47	chr4:10459132-10459182	HRCEpiC	kidney:	n/a
48	chr4:10459128-10459178	HIPEpiC	eye:	n/a
49	chr4:10459141-10459191	RPTEC	kidney:	n/a
50	chr4:10459132-10459182	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:10117460..10124392-chr4:10456675..10465032,17	K562	blood:
2	chr4:10114078..10122203-chr4:10455501..10461954,12	K562	blood:

Variant related genes	Relation type
ZNF518B	TF binding region
ZNF518B	CpG island
ENSG00000223086	Chromatin interaction
ENSG00000071127	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv997941	chr4:9805223-10493388	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	54 gene(s)	inside rSNPs	diseases
2	nsv1008649	chr4:9805223-10589802	Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
3	nsv1000587	chr4:9805223-10610752	Flanking Active TSS Enhancers Genic enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
4	nsv537022	chr4:9805223-10610752	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
5	nsv1003454	chr4:9805223-10710990	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
6	nsv537023	chr4:9805223-10710990	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
7	nsv1004801	chr4:9814720-10674528	Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
8	nsv537024	chr4:9814720-10674528	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
9	nsv931483	chr4:9814721-10716463	Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
10	nsv1009972	chr4:9903566-10710990	Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
11	nsv537027	chr4:9903566-10710990	Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
12	nsv1010620	chr4:9937123-10686682	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
13	nsv530280	chr4:9947818-10940041	Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
14	nsv869057	chr4:10013411-10875454	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
15	nsv997936	chr4:10040713-11009045	Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
16	nsv1000177	chr4:10212245-10557776	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
17	nsv537037	chr4:10212245-10557776	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
18	nsv829858	chr4:10300236-10492716	Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
19	esv2757921	chr4:10343699-10545800	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
20	esv2759223	chr4:10343699-10545800	Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Weak transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
21	nsv593727	chr4:10397327-10694991	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
22	nsv517971	chr4:10399068-10893253	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
23	nsv878694	chr4:10407572-10783606	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
24	esv1811736	chr4:10454409-10467939	Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	n/a
25	esv3327627	chr4:10457679-10460227	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	n/a
26	esv3524208	chr4:10457904-10460002	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	n/a
27	esv3524209	chr4:10457904-10460002	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10457400-10459200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr4:10457400-10459200	Active TSS	GM12878-XiMat	blood
3	chr4:10457600-10459200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:10457600-10459200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr4:10457600-10459200	Active TSS	Fetal Brain Female	brain
6	chr4:10457600-10459200	Active TSS	Right Ventricle	heart
7	chr4:10457600-10459600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr4:10457600-10459600	Active TSS	Brain Inferior Temporal Lobe	brain
9	chr4:10457600-10459600	Active TSS	Fetal Kidney	kidney
10	chr4:10457600-10459600	Active TSS	Rectal Mucosa Donor 29	rectum
11	chr4:10457600-10460000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
12	chr4:10457800-10459200	Active TSS	H9 Cell Line	embryonic stem cell
13	chr4:10457800-10459200	Active TSS	Breast Myoepithelial Primary Cells	Breast
14	chr4:10457800-10459200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr4:10457800-10459200	Active TSS	Brain Anterior Caudate	brain
16	chr4:10457800-10459200	Active TSS	Thymus	Thymus
17	chr4:10457800-10459200	Active TSS	K562	blood
18	chr4:10457800-10459400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
19	chr4:10457800-10459400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
20	chr4:10457800-10459400	Active TSS	Duodenum Mucosa	Duodenum
21	chr4:10457800-10459400	Active TSS	NHLF	lung
22	chr4:10457800-10459600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr4:10457800-10459600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr4:10457800-10459600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
25	chr4:10457800-10459600	Active TSS	A549	lung
26	chr4:10457800-10459600	Active TSS	HSMM	muscle
27	chr4:10457800-10459600	Active TSS	HSMMtube	muscle
28	chr4:10458000-10459200	Active TSS	Brain Angular Gyrus	brain
29	chr4:10458000-10459200	Active TSS	Duodenum Smooth Muscle	Duodenum
30	chr4:10458000-10459200	Active TSS	Rectal Mucosa Donor 31	rectum
31	chr4:10458000-10459400	Active TSS	Aorta	Aorta
32	chr4:10458000-10459400	Active TSS	Liver	Liver
33	chr4:10458000-10459400	Active TSS	Brain Cingulate Gyrus	brain
34	chr4:10458000-10459600	Active TSS	Pancreatic Islets	Pancreatic Islet
35	chr4:10458000-10459800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
36	chr4:10458000-10459800	Active TSS	Fetal Lung	lung
37	chr4:10458200-10459200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr4:10458200-10459200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
39	chr4:10458200-10459200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
40	chr4:10458200-10459200	Active TSS	Primary T helper naive cells from peripheral blood	blood
41	chr4:10458200-10459200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
42	chr4:10458200-10459200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
43	chr4:10458200-10459200	Active TSS	Fetal Intestine Large	intestine
44	chr4:10458200-10459200	Active TSS	Fetal Thymus	thymus
45	chr4:10458200-10459200	Active TSS	Placenta Amnion	Placenta Amnion
46	chr4:10458200-10459200	Active TSS	NHEK	skin
47	chr4:10458200-10459400	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr4:10458200-10459400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
49	chr4:10458200-10459400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
50	chr4:10458200-10459400	Active TSS	Primary T cells from cord blood	blood

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