| Tag | Content |
|---|
EnhancerAtlas ID | HS134-02892 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:114688070-114689170 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr1:114689127-114689142 | TGAACTTTGACCCCT | - | 7.51 | | Hnf4a | MA0114.3 | chr1:114689125-114689141 | TTTGAACTTTGACCCC | - | 7.81 | | NR2C2 | MA0504.1 | chr1:114689127-114689142 | TGAACTTTGACCCCT | - | 6.99 | | Nr2f6 | MA0677.1 | chr1:114689127-114689141 | TGAACTTTGACCCC | - | 6.68 | | Nr5a2 | MA0505.1 | chr1:114688900-114688915 | TGTGGCCTTGAACTC | - | 6.65 | | Rxra | MA0512.2 | chr1:114689127-114689141 | TGAACTTTGACCCC | - | 7.52 |
|
| | 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 |
| GH01I114145 | chr1 | 114688381 | 114688650 |
|
Enhancer Sequence | TGTGGAACAT GTATGTAACT TGGGAACAAA AAAACATATA TTGGAGGTAT TAAGTTTTTT 60
TTTTTTTTTT TTTTTTTTAA CCTGTTATGA GTTCATGATC TAAATAATTT GGAGACTCTT 120
TCTTCAGGTC TTTATCCTAG TGGGCTCACC AGGGAAGTCA CCACAGCTAT ATGTGTCCTT 180
ATTCTACATA TCTGGCCATC TCTAGCCCTT CACATCTGTT CTCTGTTACA GCTGTTCTGG 240
ATGCATTCTC TGCAATATGA GTCACCTCAA AACAAAAGGT GTTTCTAGGG CTTTGCTTTC 300
CTTTGATCAT ACATCTTACT TGTTCTGGTA ATAATTAGAA TTTTAATGAG AAGGGGAGTA 360
GGGGGAATCT AGAGAGCATA GAGTGCATTT AAATGTTCAG CCTGACAAAT AATTGAATTC 420
GTAAATGAAA AGAGAGGTAG GAGAAGGGGG TGGGGCAGGA CAATGAGGTT TTCCTTGGTG 480
TGGTTGCTAT TTAGATTGCC TCTCCATGTG ACCCCCAGCT GCTGTTCCCT CAGAGCTGTG 540
ATTAGGGGAG GCAGAGGGCA TGGTTTTTTG GAATCAGCAC CCAGCACTCA ATACTGGTTA 600
TATGAGACCA GGAGGCCCGT CCTATGCCTG AAGAATCTTA TTGCAGGACT AGAGGAGCCT 660
GGGCTTTTGA CATCTCACTG GCAGGCAGTG CAAGGAGAAT TAGGTCTCAA ACACTGAGTG 720
GGTTTGTCTT CACAGGAGAT GCAAGGTTGG TGAGCAAGGC TAGTAAGACC AGAAGCAGGC 780
AGCAGGGAGG AGGTGACTGT AGAAGATTCA GCTCATTTAA AATCACTGTA TGTGGCCTTG 840
AACTCAGACA TCCCTCATCT CCTAGTTTAA GTTACATTGA GATTAGAAAG GGCTGTAGGC 900
TTCTGTACAG CCTAAGGGCT GCATAAAGGC CCAGATAACC TAAGCTGTAT GCCTTCCCAC 960
TCTGGGCTTG CTGGGGCCAA CCCACTGGGA CATGTCCCCT AGGAAATCAC AGGTGCACAA 1020
ATAGCCTTCA AAACCCTTTT CCCATTCACA TCTTGTTTGA ACTTTGACCC CTTGAGGCAG 1080
CTAGAACTTT GATGGGCAAC 1100
|
