| Tag | Content |
|---|
EnhancerAtlas ID | HS092-25182 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr2:191656150-191657560 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr2:191656892-191656908 | GGCAATGTAAACAATC | + | 6.1 | | Foxa2 | MA0047.2 | chr2:191656893-191656905 | GCAATGTAAACA | - | 6.07 | | POU2F2 | MA0507.1 | chr2:191657289-191657302 | ACATGCAAATAAA | - | 6.17 | | PRDM1 | MA0508.2 | chr2:191656806-191656816 | TCACTTTCAC | + | 6.02 |
|
| | 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 |
| GH02I190791 | chr2 | 191655907 | 191658721 |
|
Enhancer Sequence | TAGAATAACT GATATTTTAA AATATGTATT TCTTTCTAAG AAAGCACGTC CTGCACAGTT 60
TTCCATTTTG AATCTGTTTT TCCCCACACC ATTAGAAGAA AGCATGGAAA ATTTCACAAT 120
CATCTGCATT CTGTTTACAG CAAATATTTT TTCATTTCAG AGTGAAATTC TCAAGCCCCA 180
AATGGGTAGG TGTTTTAATT CAGCATGGAA ATAAAGAGTT GCTTTTTCTG GACATATTCC 240
CTTCCTTTTC CTGGCAGTTA CTGGTACCGA CTTGCTCTTA ATTATCTCCC ATTCAATGCT 300
AGTCATAACC ACCCGCCCAC TTCACACTTA GGCAGTCCTG CCCACAGCAC TCACCCCAGC 360
CCCCTCAGGC TGAATCATCA GCTCCCACCC CCGTCCTTCC TTTCCCACTG CCATTTCCTT 420
TTTCGCTTCA ATGCCCTTTA TAGAGGGACA TTCTTGCTTT TCCAAAGCTT TTTTCCTCAT 480
TCCTTATTAC ATCCCCTTTA AATTTTAGAA AAACCGTAAT TCTTATGGAA TTTAATTTTC 540
TTCTCATCAC TGAGGATGAT TTGTGCTTGA TGCACCATAG AATCTGTGTT CATTAGTTAC 600
CCATTAATTC TTGTGTACTT TAGGGGGACA GTAGAATTTG AGAAACTGGA AATCTATCAC 660
TTTCACTAAA ACATACATAA GATGAAACTG AGTCACTTTG GAAGTTTCCA CCATGGCAGA 720
GACAAAGGAA GTCCCAGGCC TGGGCAATGT AAACAATCAA CTTACAGTTT GACATTTCTG 780
CTTTCAACAT TCCACTCTCC CTGATTTTTT TTTTAATGCT ATAATTAAGT CCTTTCAAAT 840
TGCTAACCCT AGAGCCTCTC TTTTTTCTTA GGCATACAAA GTATGGGAAG CTGAGGGCTC 900
TAGAATTTGA CACCTGCAGG TATCCTAGCT CTGATCAACC CACAGATATG TTGTACTGAT 960
ACCAGCCCAG GCCATGAAGA CACCATTAAA CATTCCACCC CTATGTGGTT TTTACTTAAA 1020
GTACTCTAAT ATTGTCAGGA GGTATCCATG TATGAAGACA TATTTCTCCG CATGTTCAGG 1080
ACAAGTCATT CCTTATTATC TCATGAAGAT TCTGCATACA GGTCTCACAG CTACCCCCAA 1140
CATGCAAATA AAGAAAAGAA GACATCAAGT TCAAATGATC ACTGATGGGG TTTCCTTTTG 1200
TTATGAAGCT TAGAGTTAAA AGAGATACAC TTGGGCCAGG CGCGGTGGCT CAATGCCTGT 1260
AGTCCCAGCA CTTTGGGAGG CCGAGACAGG TGGATCGTTT GAGGCCAGGA GTTTGAGACC 1320
AACCTGGCCA ACATGGCGAA ACCCCATCTC TACTAAAAAT ACACAGACTA GCTGGGCGTG 1380
GTGGTGCCCA CCTGTAATCC CAGCTACTTG 1410
|
