| Tag | Content |
|---|
EnhancerAtlas ID | HS092-35279 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr7:55063060-55064270 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXF2 | MA0030.1 | chr7:55063867-55063881 | ATTGTTTACCTTGG | - | 7.22 | | IRF1 | MA0050.2 | chr7:55063988-55064009 | TTCCTCTTTCTCTTTCTCTCC | + | 6.29 | | SPI1 | MA0080.4 | chr7:55063985-55063999 | GACTTCCTCTTTCT | - | 6.21 | | SPIC | MA0687.1 | chr7:55063985-55063999 | GACTTCCTCTTTCT | - | 6.67 | | ZNF263 | MA0528.1 | chr7:55064016-55064037 | TCCTCTCCCCCTGCATCCCCC | - | 6.38 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I054994 | chr7 | 55062600 | 55064548 |
|
Enhancer Sequence | TGGTTGGCTG CCCATCCGAG CTCTGTGCTT GTCACATGGA AGGTGCTTGA TAAATAAATG 60
TTGGATGAAT AAAGAAATGT CACTGAGAAG CATTTACATT CCTTGATTAC AATACATCAC 120
TTTAGAAATA CTCATTTCAA TCTACAAATG CTCCACAGAA AGATAGATAC AAGGACATTC 180
ATTTATCAGA GGGACAGGAA AGGTGGAAGG AGGTAACCAA CATTGATTGA GCAACCATCA 240
TGTACCAAGA GCTTTAATTT TCACAATGAT ATAGTAAAAC AGGAGTGATT AGGTCTCACT 300
TCACTGAGGA AGAAACTGAG GTTGAGTAAC TTTCCAGTTT TATGCAATTA GTGGTAAGCT 360
GAGCTGAAGC CTGAGCTTCA CATGCCATGA CTTGGATGGG TAAGCTTCAA TTACTCTCAC 420
TTAAAGGCTA GCTCATGTGT TGTCAGGGAT GCTCAGTGGG CCAGAACCAA TAATTGGGTT 480
CCAAAGGGAA TAATTAAGAT TGGAGCAAAA CCTTGTAGAT TGGGGCTGAG TCAAGTCTGA 540
ACGTCAAAAC AGAGAGACCA GGTTCAAAGA GCAGACGTGG AATCATAAAA ACATAGAATC 600
AAAAGACAAG AGTCCCATAA AAACAGGATC TGAGTCAGTC TTCAGCCCAC TTAAATCTTT 660
CTTCCACCCC CAAACTTTCC CAAAACAGCA CTCACTAAGG TCACTAATGA CTTCAACATA 720
ATCAAATCCA ATGGGTAATA CTTTATCTTT CTCTTCCGTG GCTTCTCAGC AGCATTGGCA 780
TTCTGAGCAC TTCCGCCTTT GTGAATCATT GTTTACCTTG GGCTTCCCCG TCTTCCTTAC 840
CTATCTGTCT GCTTCATCTC AATCTTACTT GCCACTTCAT CCTCCTCCAC CTCAGTCATA 900
AATGTGGTTT CCAAGATCAA TGTGAGACTT CCTCTTTCTC TTTCTCTCCA TCTCTCTCCT 960
CTCCCCCTGC ATCCCCCCTC CCCATAAACT CATTCATTCT CCTGACTTTA AATATTATTG 1020
ACAGATTGAT GACTGTTTAA AATTTTATTT TCCATCCTAC ACCACACCTC TGAGCTTCAG 1080
ACTTGATTTT CTTACTGCCT ACTTGGCATT GCTTCTTGCA TATTTCAAGA GAAGCCCAAA 1140
TGTAAGGATT TCCAATACAA ATTCATCATC TTGATCCTCA TTTTCTTCAG TAGTCCCAAC 1200
TTGAGAATGA 1210
|
