Variant report

Variant	rs28510755
Chromosome Location	chr4:682233-682234
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:20)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:20 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	USF1	chr4:682188-682526	H1-hESC	embryonic stem cell:	n/a	n/a
2	POLR2A	chr4:681886-683772	H1-hESC	embryonic stem cell:	n/a	n/a
3	SIN3A	chr4:682164-683395	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD2	chr4:682132-682478	H1-hESC	embryonic stem cell:	n/a	n/a
5	USF1	chr4:682135-682593	H1-hESC	embryonic stem cell:	n/a	n/a
6	E2F6	chr4:681988-683594	H1-hESC	embryonic stem cell:	n/a	chr4:682298-682305 chr4:682298-682305 chr4:682294-682306 chr4:682669-682678 chr4:682298-682305
7	MAX	chr4:682005-683439	H1-hESC	embryonic stem cell:	n/a	chr4:682978-682987
8	MAX	chr4:682073-682582	H1-hESC	embryonic stem cell:	n/a	n/a
9	E2F6	chr4:681854-683709	H1-hESC	embryonic stem cell:	n/a	chr4:682298-682305 chr4:682298-682305 chr4:682294-682306 chr4:682669-682678 chr4:682298-682305
10	GTF2F1	chr4:682230-682435	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr4:682073-682663	HCT-116	colon:	n/a	n/a
12	POLR2A	chr4:682133-682568	H1-hESC	embryonic stem cell:	n/a	n/a
13	TAF1	chr4:682131-682478	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr4:682137-682599	HCT-116	colon:	n/a	n/a
15	MAX	chr4:682177-682489	H1-hESC	embryonic stem cell:	n/a	n/a
16	GABPA	chr4:682064-682549	H1-hESC	embryonic stem cell:	n/a	n/a
17	TBP	chr4:682125-682522	H1-hESC	embryonic stem cell:	n/a	n/a
18	ZNF143	chr4:682185-682738	H1-hESC	embryonic stem cell:	n/a	chr4:682524-682543 chr4:682667-682685
19	E2F6	chr4:682209-682355	K562	blood:	n/a	chr4:682298-682305 chr4:682298-682305 chr4:682294-682306 chr4:682298-682305
20	POLR2A	chr4:680810-682554	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:682184-682234	PANC-1	pancreas:	n/a
2	chr4:682184-682234	HIPEpiC	eye:	n/a
3	chr4:682184-682234	NB4	blood:	n/a
4	chr4:682184-682234	AG04450	lung:	fetal
5	chr4:682184-682234	BE2_C	brain:	n/a
6	chr4:682184-682234	Hepatocyte	liver:	n/a
7	chr4:682184-682234	Hela-S3	cervix:	n/a
8	chr4:682184-682234	U87	brain:	n/a
9	chr4:682184-682234	HEK293	kidney:	embryo
10	chr4:682184-682234	Caco-2	colon:	n/a
11	chr4:682184-682234	Jurkat	blood:	n/a
12	chr4:682184-682234	SK-N-SH	brain:	n/a
13	chr4:682184-682234	HMEC	breast:	n/a
14	chr4:682184-682234	HCM	heart:	n/a
15	chr4:682184-682234	AoSMC	blood vessel:	n/a
16	chr4:682184-682234	AG04449	skin:	fetal
17	chr4:682184-682234	HL-60	blood:	n/a
18	chr4:682184-682234	GM19239	blood:	n/a
19	chr4:682184-682234	MCF-7	breast:	n/a
20	chr4:682184-682234	HEEpiC	esophagus:	n/a
21	chr4:682184-682234	SKMC	muscle:	n/a
22	chr4:682184-682234	AG09309	skin:	n/a
23	chr4:682184-682234	CMK	blood:	n/a
24	chr4:682184-682234	RPTEC	kidney:	n/a
25	chr4:682184-682234	ovcar-3	ovarian:	n/a
26	chr4:682184-682234	LNCaP	prostate:	n/a
27	chr4:682184-682234	AG10803	skin:	n/a
28	chr4:682184-682234	AG09319	gingival:	n/a
29	chr4:682184-682234	GM12891	blood:	n/a
30	chr4:682184-682234	HRE	kidney:	n/a
31	chr4:682184-682234	H1-hESC	embryonic stem cell:	embryo
32	chr4:682184-682234	NT2-D1	testis:	n/a
33	chr4:682184-682234	HepG2	liver:	n/a
34	chr4:682184-682234	HCF	heart:	n/a
35	chr4:682184-682234	HNPCEpiC	eye:	n/a
36	chr4:682184-682234	ProgFib	skin:	n/a
37	chr4:682184-682234	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:682184-682234	GM06990	blood:	n/a
39	chr4:682184-682234	HCT-116	colon:	n/a
40	chr4:682184-682234	HCPEpiC	choroid plexus:	n/a
41	chr4:682184-682234	ECC-1	luminal epithelium:	n/a
42	chr4:682184-682234	PFSK-1	brain:	n/a
43	chr4:682184-682234	NH-A	brain:	n/a
44	chr4:682184-682234	BJ	skin:	n/a
45	chr4:682184-682234	HRPEpiC	eye:	n/a
46	chr4:682184-682234	GM12878	blood:	n/a
47	chr4:682184-682234	SAEC	small airway:	n/a
48	chr4:682184-682234	PrEC	prostate:	n/a
49	chr4:682184-682234	A549	lung:	n/a
50	chr4:682184-682234	T-47D	breast:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:680186..682717-chr4:773971..775707,2	MCF-7	breast:
2	chr4:681383..683193-chr4:698223..700658,3	K562	blood:
3	chr4:665676..669905-chr4:679525..682855,5	K562	blood:
4	chr4:680242..683670-chr4:697022..701034,8	MCF-7	breast:
5	chr4:680689..682702-chr4:985061..987897,2	K562	blood:
6	chr4:669988..672792-chr4:681146..683044,2	K562	blood:
7	chr4:681693..683683-chr4:698278..699853,2	K562	blood:

No data

Variant related genes	Relation type
MFSD7	TF binding region
MFSD7	CpG island
ENSG00000215375	Chromatin interaction
ENSG00000127415	Chromatin interaction
ENSG00000185619	Chromatin interaction
ENSG00000249592	Chromatin interaction
ENSG00000169020	Chromatin interaction
ENSG00000145217	Chromatin interaction

Extended variants
information (count: 91 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10001451	1.00[AMR][1000 genomes]
rs10006278	1.00[AMR][1000 genomes]
rs10010598	0.84[LWK][hapmap];1.00[MKK][hapmap];1.00[AMR][1000 genomes]
rs10015198	0.88[MKK][hapmap]
rs10017347	1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[AMR][1000 genomes]
rs10017435	1.00[AMR][1000 genomes]
rs10018607	1.00[AMR][1000 genomes]
rs10020292	0.93[MKK][hapmap];1.00[AMR][1000 genomes]
rs10023609	1.00[AMR][1000 genomes]
rs10024023	1.00[AMR][1000 genomes]
rs10025758	1.00[AMR][1000 genomes]
rs10027392	0.84[LWK][hapmap];1.00[MKK][hapmap];1.00[AMR][1000 genomes]
rs10028157	1.00[AMR][1000 genomes]
rs10028526	1.00[AMR][1000 genomes]
rs10028537	1.00[AMR][1000 genomes]
rs10029924	0.92[LWK][hapmap];1.00[MKK][hapmap];1.00[AMR][1000 genomes]
rs10030020	1.00[AMR][1000 genomes]
rs10035021	1.00[AMR][1000 genomes]
rs12331186	0.92[LWK][hapmap];1.00[MKK][hapmap];1.00[AMR][1000 genomes]
rs28366852	1.00[AMR][1000 genomes]
rs28399001	0.92[LWK][hapmap];1.00[MKK][hapmap];1.00[AMR][1000 genomes]
rs28413992	1.00[AMR][1000 genomes]
rs28414606	1.00[AMR][1000 genomes]
rs28436699	1.00[AMR][1000 genomes]
rs28459140	1.00[AMR][1000 genomes]
rs28477853	1.00[AMR][1000 genomes]
rs28478159	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28510278	1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[AMR][1000 genomes]
rs28527330	1.00[AMR][1000 genomes]
rs28531889	1.00[ASW][hapmap];0.92[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28538930	0.92[LWK][hapmap];1.00[MKK][hapmap];1.00[AMR][1000 genomes]
rs28540058	1.00[AMR][1000 genomes]
rs28546458	1.00[AMR][1000 genomes]
rs28551514	1.00[AMR][1000 genomes]
rs28594284	0.92[LWK][hapmap];1.00[MKK][hapmap]
rs28601829	1.00[AMR][1000 genomes]
rs28605120	1.00[AMR][1000 genomes]
rs28615478	1.00[AMR][1000 genomes]
rs28633819	1.00[AMR][1000 genomes]
rs28648652	0.91[AFR][1000 genomes]
rs28665728	0.92[LWK][hapmap];0.88[MKK][hapmap];1.00[AMR][1000 genomes]
rs28671384	1.00[AMR][1000 genomes]
rs28706206	1.00[AMR][1000 genomes]
rs28709824	1.00[AMR][1000 genomes]
rs28754367	1.00[AMR][1000 genomes]
rs28818828	1.00[AMR][1000 genomes]
rs28843467	1.00[AMR][1000 genomes]
rs28862677	1.00[AMR][1000 genomes]
rs6827034	1.00[AMR][1000 genomes]
rs6835327	1.00[AMR][1000 genomes]
rs6842140	1.00[AMR][1000 genomes]
rs73056559	1.00[AMR][1000 genomes]
rs7655485	1.00[AMR][1000 genomes]
rs7665160	0.92[LWK][hapmap];1.00[MKK][hapmap];1.00[AMR][1000 genomes]
rs7671294	0.88[MKK][hapmap];1.00[AMR][1000 genomes]
rs7680416	1.00[AMR][1000 genomes]
rs7689014	1.00[AMR][1000 genomes]
rs7696942	1.00[AMR][1000 genomes]
rs9990446	1.00[AMR][1000 genomes]
rs9991058	1.00[AMR][1000 genomes]
rs9994679	0.92[LWK][hapmap];1.00[MKK][hapmap];1.00[AMR][1000 genomes]
rs9995112	1.00[AMR][1000 genomes]
rs9996316	1.00[AMR][1000 genomes]
rs9996400	1.00[AMR][1000 genomes]
rs9997898	0.93[MKK][hapmap]
rs9998466	1.00[AMR][1000 genomes]
rs9998594	1.00[AMR][1000 genomes]
rs9998776	1.00[AMR][1000 genomes]
rs9999833	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011715	chr4:43860-823487	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	nsv931097	chr4:72447-683874	Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats 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 lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv532702	chr4:72447-755236	Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
4	nsv1005224	chr4:507005-900281	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Strong transcription Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
5	nsv536976	chr4:507005-900281	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	nsv878245	chr4:509178-694613	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
7	nsv822425	chr4:540105-1413799	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
8	nsv878246	chr4:592507-696848	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
9	esv2757916	chr4:603208-931354	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
10	esv2759217	chr4:603208-931354	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
11	nsv878247	chr4:607202-925149	Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
12	nsv530490	chr4:614355-1399150	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS 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	104 gene(s)	inside rSNPs	diseases
13	nsv593206	chr4:625962-735150	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
14	nsv878248	chr4:645300-685993	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
15	nsv878249	chr4:649639-691026	Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
16	esv1829397	chr4:655939-1041957	Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
17	nsv829834	chr4:665477-775524	Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
18	nsv10413	chr4:667204-684301	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
19	nsv593208	chr4:668000-682233	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
20	nsv878250	chr4:668567-683842	Active TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
21	nsv878251	chr4:669857-683842	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
22	nsv878252	chr4:669857-685993	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:675200-682400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr4:675200-682600	Weak transcription	GM12878-XiMat	blood
3	chr4:675400-682400	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr4:677000-682400	Enhancers	Fetal Muscle Leg	muscle
5	chr4:677800-682400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr4:678200-682400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr4:678400-682400	Weak transcription	Brain Cingulate Gyrus	brain
8	chr4:678400-682400	Weak transcription	Brain Substantia Nigra	brain
9	chr4:678400-682600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:679200-682400	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr4:680200-682400	Enhancers	Placenta	Placenta
12	chr4:680200-682400	Enhancers	Stomach Mucosa	stomach
13	chr4:680400-682800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr4:680400-683000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr4:680600-682400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr4:680600-682400	Enhancers	Fetal Intestine Small	intestine
17	chr4:680600-682400	Enhancers	Psoas Muscle	Psoas
18	chr4:680600-682400	Enhancers	Right Atrium	heart
19	chr4:680600-682400	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr4:680600-682400	Enhancers	Spleen	Spleen
21	chr4:680600-682400	Flanking Active TSS	HepG2	liver
22	chr4:680600-682600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr4:680600-682600	Enhancers	NH-A	brain
24	chr4:680600-682800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr4:680600-683600	Enhancers	Placenta Amnion	Placenta Amnion
26	chr4:680600-684000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
27	chr4:680800-682400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr4:680800-682400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr4:680800-682400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr4:680800-682400	Flanking Active TSS	Colonic Mucosa	Colon
31	chr4:680800-682400	Enhancers	Fetal Intestine Large	intestine
32	chr4:680800-682400	Flanking Active TSS	Hela-S3	cervix
33	chr4:680800-682600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr4:680800-682600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr4:680800-682600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr4:680800-682600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
37	chr4:680800-682600	Enhancers	HUVEC	blood vessel
38	chr4:680800-682600	Flanking Active TSS	NHDF-Ad	bronchial
39	chr4:680800-682800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
40	chr4:680800-682800	Flanking Active TSS	Adipose Nuclei	Adipose
41	chr4:680800-682800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
42	chr4:680800-682800	Enhancers	NHLF	lung
43	chr4:680800-683000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr4:680800-683800	Enhancers	Primary B cells from cord blood	blood
45	chr4:680800-683800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
46	chr4:681000-682400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr4:681000-682600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr4:681000-682800	Flanking Active TSS	Duodenum Mucosa	Duodenum
49	chr4:681000-682800	Flanking Active TSS	Osteobl	bone
50	chr4:681200-682600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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