| Tag | Content |
|---|
EnhancerAtlas ID | HS002-00799 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr1:161186060-161187770 |
SNPs | | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr1:161187349-161187360 | TTCTGTGGTTT | + | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CACTGCACTC TAGCCTGGGG GACAGAGTGA GACTCCGTCT CAAAAAAAAA AAAAAGATTT 60
TACATATATA TCTCTATCTA TCTATCTATA TACACACACA CACACATACA CACACACACA 120
CACACACACA CACACACACA CATATATATA TATATATAGA GAGAGAGAGA GAGAGAGAGA 180
TAACCCTTTA GGAAGGTAGG ACTCTGTTCT TGTGCTTGGG AGTAAGGCAA GGATATAGCC 240
AAGACAAACA GACGGGATTG CTGTTTCTAT GGGTCATTGT TAATGCTCCA TTCTGTCAGC 300
AGTTGATAAT GAGGGTGGGC AGCATGAGAT CCCCAGTTCC AGAGACCTGA GCGTCAGCTG 360
AGAAATAGAG GCAGAAATGG GAAGGTCTCT GAAGCTCTAC AGCTCCAGCC ACTATCTAAG 420
AATTCTCACT CCTCGTTCAC TCTGTGTTGT CTGTGCTGGA TTGGTGTGTG TGTGTTGGTG 480
GCAGCTGGGT GTTGGGGAGG AGGAGGTCAG TAAACTTCAG GGAAACTGTG GAAATTGAAA 540
GAGAATGACT GGGGAGGAAT TCCAGCAGCC TAGCTGAGAA GGTGGGAGCA AGTATTAAGT 600
TAGCCACTGG TCTGCTGCCG TGGGATGAGG AGGGAGGAGG CCCGCTGAGG CACAAAGGAA 660
AGCATGGGCT TTAGAGGCAG AAAACCTGCA TTTGAGTTCC AGCTCTGTCA CTTAACTCTG 720
TGGCTCTGAG TGAGTTACTT AGCTTTTCCG AGCCTTGGTT TCGTCACCCA TAAAATGGCG 780
ATGATGATGT TTCCCTCACA GGGTAGTTTT AAGATTTGTG CAATATCGTG TGTGTGAAAG 840
AGTGTTGCAG AATAAAAAGT ACTTGACCGA TGTCAGCAAT TGACTGACGT TAGTCACATG 900
TTCCCTACTG GTCCTCTGAT ACGGGGTGAG AGCAGTCTCT GGAGCCCAGA CTTGATTTGA 960
TTTTTTAAAT TGCACAAAAC TTCCCCTCTC AGAGACCCAG AGAGTGAGTA ATAGGGCAGA 1020
GTAACAGGAG CTGGAATCCA TATAGCTGTG GTCATTCCCC CAGCCTTGTG TTCAGGGCCA 1080
AAGGTATCTG TAAGGTCTGG GAAAAACAGA CACACTTTTT TTTTTTTTTT TTTTTTTTAC 1140
ATATTTAAGT GTCTTGTGGT GGGACAGAAA GCAACAAGGC TGAGGCTAGG AGATGACCAA 1200
TGATAGAGTA ATTGCCTTCT CTCCCTTCCC CAGCTCACAT CCTTCCTGTC CAGCCCTCAG 1260
CCACAGGTCA CAGGACTTAG TAGAGACACT TCTGTGGTTT CTTCACTGAA ATTTGCCACT 1320
ACCTCTCCCT CCCACTACCC ATCTTGGCTG AGGTTTTGGT TTCAGTCCAG TGGACTCAGA 1380
TGGGTCCCTT GAGGTGGATA AAGTGCTCAA TGGTGCCTGA AGAACCCACA GTGCTAAAAA 1440
GAAAAGGTTG GGGGCTGAGG GGGAAGGCCT CAATTATTAG TCCGTGTGAG TCCCATTTCA 1500
ATAGAACCCT CAAGCTTCCT ATCCTAGCCT GACCCTATGG TGTGGGAGGA GGGAAAGGTA 1560
AGGGCAGTGG AAGGCCAGAG AGAAACAGAA TTTCTTCCCT TAGACGGCTC CCCTCCAGGC 1620
CCTGTCCTAC CTCCCAGAGC CCCTTCCCTT CTCTCCTCTG AGTACCAGAT CCTCCCTGAT 1680
ACCCCCGACC CCATGGGCAT CCTCTATCCC 1710
|
