| Tag | Content |
|---|
EnhancerAtlas ID | HS134-05129 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:225033710-225035060 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr1:225035031-225035046 | AATTAATCATTAATT | + | 6.34 | | HNF1A | MA0046.2 | chr1:225035031-225035046 | AATTAATCATTAATT | - | 6.47 | | TFAP2A | MA0003.3 | chr1:225034771-225034782 | TGCCTCAGGCA | + | 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 |
| GH01I224846 | chr1 | 225033870 | 225035012 |
|
Enhancer Sequence | CTTCAGGCCA TCTGGATGTA TACATGCAGG TCACAGAGGA TATGATGGCT TAGCTTGGGC 60
TCAGAGGCCT GACATTATAT GCCCCTCCAG GCTACCAAGG CTATGTCAGT CATCTCTGTA 120
GCCCCCATGC CAGCCCACAT ACTTGCTGCC CAGGACTGTC TTGGAGAGAC TTGGAATAGC 180
TCTGGGTGCT CTTTGGCAGA AGATCCCTGG CTGAGACACT GCAGTAGGAG CCAGGCCCTT 240
AGGGGACAGC CAGCAGAGTA AAGGCTCAAC TGGCCAGAGC CCTGTGTGAT GCTTAGTTCA 300
GGACAGCCCT GCTGAAATTG CTGGGGGCAC TAATGAATCC AGTAAATAAA TCATTGTCAG 360
ATGGAGCTTA GCTGTTCTCC TTGGAAATTG GCCACGGTCA CAATGCAAGC AGTACCAGAT 420
GTGTCAGGGT GTCATACTCC AAGTATCAAA AAAATCAGTC TTTGTGGATA AATATCACAA 480
ACCAAAAATA AAATTCTAAG CTCTCCCAAC CACCAGAATA GACCCTCCCC CTCCTGGCCA 540
AGATACCCCA GAGAAATCTG AAACACTAAA TTCCAGGTCA CTGATGGAAG GGAAGTTGGA 600
CATACCTCTC CCTCTTGGAG TTTAGGCACA AATGACCAGC ATTAACATTA AAATAGAGAC 660
AGAAGACTGA CAAAACAGGC TCTTTGTGGC AATAAGATAA CAAATTCCAA CCTGACTCTA 720
GTATAGCATC ACATGCTGTC TGAGGGCTGC TAGCTAAGAG ACTTCATCTA CACAACAAGG 780
GCCTTGGCTT CCACCACCCT GTTATCTTAG CTCAAATATT CCTTGCTACC GATTTCTTAA 840
GTCTTTAGAC AAAGCTTAAC TTTTTCAAAC AATTGCCAAT CAGAAAATCT TTGAATCCAC 900
CAATGACCTA TCTACTTCCT CCCCCAAACC CCTGCTTACC CACCACCTTT GAGATGTCCT 960
GCCTTTCTTG TAAACCAATG TATCTCTTAC ATATATTGAT TTATGTCTTT GCCTGTAACT 1020
TTTGTCTCCC TAAAATGTAT AAAACCAAAC TGTAACCTGA CTGCCTCAGG CACATTTTCT 1080
CAGGACCTCT TGAGGCTGTA ACACAGGCTG TGGTCACTCA TATTGGCTCA CAATAAGCCT 1140
CTTCAAATAT TCTGCAGAGT TTGATTTTTT TGTTAATAAT ATATGGGATA AAGGATGTGA 1200
TGCTATTCAG TTCCCAAGCC TGTGCACCCT TGAGGGCTGT GAGGCCAAGC CAGCTAGTCC 1260
GATTTATAGT GACTCTGTTT GCTAACATCT AAGGACTTTT TATCTATAGC ATTCAGTTGC 1320
TAATTAATCA TTAATTGATA ATTAGTATTT 1350
|
