| Tag | Content |
|---|
EnhancerAtlas ID | HS048-26424 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr3:141656080-141657220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr3:141656537-141656548 | TTCTGTGGTTT | + | 6.32 | | Zfx | MA0146.2 | chr3:141656083-141656097 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | 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 |
| GH03I141937 | chr3 | 141656083 | 141657614 |
|
Enhancer Sequence | CCACCCGCCT CGGCCTCCCA AAGTGCTGGG ATAAGATGTG AGCCACTGTG CCCGGCTCAC 60
TGCAACCTCC GACTCCCTGG TTCAAGCGAT TCTCCTGCCT CAGCCTCCTG AGTAGCTGGG 120
ATTACAGGCA CATGTCACCA CGCCCAGCTA ATTTTTGTAT TTTTTGTAGA GACGAGGTTT 180
CACCACGTTG GCCAGGATAG TCTCGATCTC CTGACCTTGT GATCCACCTG CCTCGGCCTC 240
CCAAAGCGTT GGGATGACAG GCGTGAGCCA CCGCGCCCGG TGTGCCCGTT TTACCAACTG 300
CTGCAGCTGC TGCTGGTTTT CTCATCCCCT CGGCTGAACC ACCAGCCCCT CCCTCAGCAC 360
CTGGAAGGAG AAATCTGGCG TCTTGCTGGC GGGCTACTGC CCTGCAGCAC CTCCATGGCT 420
CCCTGGCTGA TAACATAGGG GTGTTGTAAA CTTACATTTC TGTGGTTTTC TGCTCATGTT 480
GTTTCTCCCC AGACTTTTCT CCCATCTGCT TCTGTGTTAT CTTTTGTTAC GATGACAGGG 540
AGTGGTCCCT GCCTGCCCTG GCAGGCACCT GCCTCCCTGG CCAAGCCCCA GCCCAGGAAG 600
TTGCTCATGC TGGGCCCTCC AGGTTCTGAG AAAACTTTCA GGGATTGGGG TAGGGAAGAA 660
AATAGGTGAA AACCCTCTCT CCTCTGCAAG CTTATTTCTT TGGCCTGGCC TGTCTTTAAC 720
CTGCACAGTT TATGTGTAGA CAAGTCTCCC GGTGCGGGCC CAGCAGGCAG GTGACAGCCG 780
CCCTTGCGGG AGTCATCCTT AACCAAGCAG TTTCAGAAAT GTTTCTTGAG AAACTGTTTC 840
CGGAAGTCCC GGAGCCTGTG TTGCCCATTG ACAAGCCTTG TCGGTCTCAG AAGACAGACT 900
CCGGGGGTCT ACATCCAGAG ACCCGGCTGA GGACTGAAGC CCGGGGTTTC CAAGCGGCTG 960
CCTTCTCCGT CCTGCAGCAG GGTGCGAGTC AACCGCCCTG GCTAAGGGAG CAAGGAACCC 1020
CCGCCATGCT GTGTCCCCTC CCCCCATTCC CCGAATGCCC GTCTGTTCAA AGAGGGTGAG 1080
AGGAGGGGGG AATACCAACT GCTCCGAGGA AAATGCAGTT CATCATATGC ATCTTTGCAC 1140
|
