| Tag | Content |
|---|
EnhancerAtlas ID | HS052-02788 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:170276210-170277580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYB | MA0100.3 | chr1:170277032-170277042 | ACCAACTGTC | + | 6.02 | | RARA | MA0729.1 | chr1:170276854-170276872 | GAGATGAAAAGGTCACTG | + | 6.35 |
|
| | 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 |
| GH01I170306 | chr1 | 170275922 | 170277235 |
|
Enhancer Sequence | AAGAAAGCAA CCCCCTCCCC CCCCAAAAAA AACACACGGT ATACCCCTCT GATCCCATGC 60
TAGCAGCCCT CCTGGGAACA GCTTACAAGA TAAGACAGCT TTGCAACAGA GCACTATTAA 120
CTCTCTCCCT TTTGTCGCTC TTCTCAGTGA GGCTCTTTAC TGGGGTGCAA ATGCCCTATT 180
TTGTAGAAGA GAATTGACAC TGTGCATAGC AAATACAAAC AGCAAAGTTA TTCTGACAAA 240
CTATGTAAGC CAATGTCCTC CTCTTTGATC CATTTTTTTG TGTGTGTGTG TGCCTAATTG 300
TTGGCAGGCC AATAAAGCTC AGAGTCTGTG GCACTGGAAG AAAGAGGTGC AAGAAGCCTG 360
CAAGTTTATG CTGTCAGGGG AGGATTTCTG GATTCCCAGC ATTAAAGGAT TTGAATCCCC 420
TGGCTGCTTT GGGAAAGTGT CCTGTTTGTG TTGGGGGAGT CCCAGGGCAG ACTTCCATTA 480
CAGAAATTGA GAGATGTTGT TGCCTTAGGC TCCAGCACCT TTCCCAGGCT TGTTACATGC 540
CATTCACTCA TTCCTTCATT CAACAGATAT TGATGAAACA CCCCTGACTC AGAGCTGGGG 600
AACATGTGAG GCCAGGGAAG GCAGTATGCT AGGAGTTGTC TTAGGAGATG AAAAGGTCAC 660
TGACCCTGAC CTTGAATAAG CAGAACTGTG TCATGGACAT AAGTAATGCA GATATTAAAG 720
TCAATGTTAG GACGATAAAT TAGAGTCACT GTTAGGACAA CATAATAATA AAGACAAGGT 780
TAACTATTTG GGGAAATAAT ACAGACTAGC AGGCAAAGGC CCACCAACTG TCAGAAAGTT 840
TTGAGTCCAT GTCCTAGACC CTCCATTTTC TAATACCACC TTGGGCATGC CATTAACTTC 900
CATGAGGTTC AGATACAGAG AACAATGCTC ACCTCATAGG GTTATTATGA GCCTTAAATA 960
AGGTAATGCT TTACTTAGCA CATTATTGTC TGTGTCACAG TAACTATTAT TAGTATTTTG 1020
ATAGTCTAAT GTTAAAGCAC ATCTCTTTTC TTTCTTCAGA CCCCTAAATC AAAATAAAGA 1080
AGTATAGCTG TTATTGCAGG GGATAATCCC ATATTTAGTA AATATCTCCA GAAATCATTC 1140
TAAATAATGG AGTTGAGCCC AAGGCAACTT TGCCAAAGGG TCTTGATCTT TTAATGCCTG 1200
AAAGTGACTT ATGTTCATTA AAAACTGCTT GTTGGCCGGG TGTGGTGGCT CATGCCTGTA 1260
ATCCCAGAAC TTTGAGAGGC TGAGGTGGGT GGATCACCTG AAGTCAGGAG TTCAAGACTA 1320
GCGTGGTCAA CATGGTGAAA CCCCGTCTCT ATTAAAAATA CAAAAAATAG 1370
|
