| Tag | Content |
|---|
EnhancerAtlas ID | HS088-00970 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr1:23999290-24000460 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:23999620-23999641 | AAAAAAAAAATGAAACAAAGG | - | 6.66 | | REST | MA0138.2 | chr1:23999755-23999776 | GGCACTGTCCTTGGTGCTGAG | - | 9.24 |
|
| | 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 |
| GH01I023673 | chr1 | 24000081 | 24000230 |
|
Enhancer Sequence | TGATCATGCC ACTGCACTCC AGCCTGGATG ACAGAGTGAG ACCCCGTCTC GGAAAACAAA 60
AAACTGCCAT AATTAAGAAT GTTAACTCTA CTAAAAAAAT TAAAACCTGT CATAAGCATC 120
TTGGTAAATA AATCTTTCCA TGTGTCTTTG GTAGTTTAAT TATAATCAAC TCCTAATGAA 180
ATAAATTCCT CATGAACCAC TGGGCATGGT GGCTCAAATC TGTAATCCCA GCACTTTGGG 240
AGGCTGAGGC TGGAGCATTA CTGGTGGCCG GGAGTTCGAG ACTAGCCTGG GCAATGTAGC 300
AAGACCCTGC CTCTACAAGA GTTTCATTAA AAAAAAAAAA TGAAACAAAG GGTAGGCATT 360
ATTTTTGGAA TCTTCTGACA CAGACTGCCC AATTGCCCTT GAGAAAAGAC TAGACCTGCA 420
GGGGCAGGGT GTCCCTTCAA ATGGTGACTG AGCGCCAGTG TGCCGGGCAC TGTCCTTGGT 480
GCTGAGAGTG CCGCAGTGAA TAAGAAGCAA CTCTGCTGTT GGAGCTCAGT CTCCTGGGAG 540
ACTGGGAAGA GATAAGGCAG ACGATGACAA GTGCTTCAGA AAATTCTACA AAAAGGTGAA 600
GGGACACAGT ATGGGAGAGT TACTGTACAT CAGGTATTCA AGCAGGGGTG GGCTCTGAGA 660
TAACATTAGA GCAGAAACCT GAAGCTTCAG TGCCTGTTTC CCATAACCTG AGTATTATCA 720
CACATCTCAG CTAGTGAGAC ACATGAGTTT CATCCCCACG TCCTCCAAGC ATTTATTACA 780
CACCTACTGT ATTCTAGATG CCAAAAGAAC AAAGCATGTT AGCCTGCAGC TAGTGAACTA 840
GATATTCAAC TTGTAGTTTG CTGACCTCAT AGGCTTGTAG TAGCAGGACC ATGGATTGGC 900
ATAGAACCAA GTGAGTCACC AAGTTCATCA AACCAACGGG TAAAGTTCAT CACTACCTCA 960
CCCTCACTGC AGGCTCAGTG GGAAGAGGCT TGTATTTGAG TCTGGGGAGT TGGTCTCATT 1020
TTCAACTTCT GATCTGGTCA TTTGCCAGTC ACTGGGCCTT GGGCAACCCA CTTCTGATCC 1080
TCAATTATCC TTTCTGAGAA AGAAAAATAT TCCTTTTACA AACTTGAATT ATTTATGTAA 1140
AAGTGCTTAC TAAAAAATGC TTTCAAAGCC 1170
|
