| Tag | Content |
|---|
EnhancerAtlas ID | HS047-27377 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr5:125701100-125702230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GRHL1 | MA0647.1 | chr5:125701415-125701427 | AAAACCGGTTTA | - | 6.44 | | GRHL1 | MA0647.1 | chr5:125701415-125701427 | AAAACCGGTTTA | + | 6.92 | | STAT1 | MA0137.3 | chr5:125701407-125701418 | TTTCCTGGAAA | - | 6.62 | | Stat4 | MA0518.1 | chr5:125701404-125701418 | TTTTTTCCTGGAAA | - | 6.02 | | TFCP2 | MA0145.3 | chr5:125701416-125701426 | AAACCGGTTT | + | 6.02 | | TFCP2 | MA0145.3 | chr5:125701416-125701426 | AAACCGGTTT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr5 | 125701766 | 125701858 | | chr5 | 125701796 | 125702121 | | chr5 | 125701200 | 125701395 |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH05I126366 | chr5 | 125701301 | 125701450 | | GH05I126365 | chr5 | 125701641 | 125701790 | | GH05I126368 | chr5 | 125701796 | 125702121 |
|
Enhancer Sequence | GAATATGCAA TAACCACTAT GCAATTTGAC AGATAATAAT GCTATTGAAA TCAAGAATGC 60
TGCTTTTTAA AATCTGGTAA CTCTGAGGTC AAATGTGTAT GTTTTATCAA ACACCCAAAT 120
GTGAATGTTT AAATGTTTAC AGCGGTGTAA GGGAGTCAGC TCATGCTTGC TCAACTGTCA 180
GTTCATTACA GGCTCAATTC CCAAAGTCAC GTTCAGTGTA TCATGTCAGC AGCTTGAAAT 240
CAGCTGTGGT AGGAGTATTT ACGCTGTGGA AATTGGCCAG TGCTACAAAT CAGAGCTTTT 300
TTTTTTTTTT CCTGGAAAAC CGGTTTACCA ATGCATCACT GTTTAAATAA TAAACATATC 360
AATCAACAGA AAGTTCTGCA AACAAAATTT TTAAAATCAA CTATCTCAAA TCATTTTATA 420
AATTTAAGCA AATATAGTTA AAAGCACTAA AAAGACTTAC CCAAGCTGGT GGATAAACTA 480
GAATAGGAAC TTGGGTTTTC AAATTTCTTA CCTTTATATC TTAAAGCCCC AAATGCACAC 540
AAAAAAAGAA AGATTATCTA AAGTCCAATC TTGCCATGTC TACTTACATG TTTACTGAAG 600
CTGCAAGATC AACTTTCTAA TCTTCTGGGG GCAAACTCCC TCTAAAGTCA TGAGCTGTGG 660
CAGATAGTAA TAGTTCTCTG ACAAGGGGAT AACATATATC CTTTCTCTGC ATCCTCTCAA 720
AGGGTTCACA ACTTTGGGAG AGAAATCAAC CCCCTCCCCT CTTTATCATA AAAACCGTAG 780
AATAAAGAAG TTTGAAGGAG AGAGGAAGGG ACTTAAGATA TGCTTTAGCC CATGAATTAG 840
ACTGGAATAT TCCAAGCTGC TTGGCAAGGT CATTATCACC AGTGTCAACA CTCCATGGGC 900
CTAGACTGTC AATGCTTGCC CTCCCTCTAG GATTAGGTCT TCCACAAACC ACGTGCAAAC 960
ACACAGCTGT TGTCCCATTG AGTAAAGCAA ATCATATCTT TCACTTATAT CATATGACTC 1020
CACTCAACAT GAGTGAAAGT ATGACCAACT CAAAGATCCT AATCTTCATT GTCATTACCA 1080
TCAGTAGTAT TTTCTGAATG CTTACTATGT ACAGGCTTCA TACTTGAAGT 1130
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