| Tag | Content |
|---|
EnhancerAtlas ID | HS176-23457 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:242620040-242621500 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr2:242620438-242620449 | GGTGACTCATC | + | 6.32 | | JUND | MA0491.1 | chr2:242620438-242620449 | GGTGACTCATC | + | 6.62 |
|
| | 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 |
| GH02I241678 | chr2 | 242618303 | 242622569 |
|
Enhancer Sequence | TCACACCACT GCATTCCAGC CTGGGTGACA CAGCGAGACT CCATCTCAAA AAAAGAAAAA 60
GAAAATTATC CCAACAATAC AACTCAGAAA TCTCATATGA CAACAAGTAC AGCACAGTGA 120
TTTGTAACCT TACTTTTAAT CCAAAAAGGT CTGGATCTTC TCTAGAAGAT GCCATACCCA 180
CACCTCCAGC AAAACCCAAC ATGGAGAAGA TAACCTTACT AAATAGTAAC AAACACAACT 240
GGTAAAGTTC AATGTTCCAG AAACACGGCA GGGGAAAGGA GATGCACTGT CAGCTGTCTT 300
GGTCAGAGAG GCCAGCTCTA CCCTGTCGAG GAAGAAGAAA GCACAGGCAA AGAAGAGAGC 360
AGAGGATGGT GGCGGGGGAA GCGTGGGCAC AGCCAGCAGG TGACTCATCC ATGCTCATGA 420
CCCCTAGCCT GGACTGCAAG GATGTTCTCA GCCAAATACC ACAAGTCCAC CATCATCCCT 480
ACAGCTGCCA AGATCACAGA TGTACAAAGA CACGGGGCCT GACACTAGTG AGAAGCACTG 540
CTCAAGACAG AGAAAGAAAA GTCCGATTCA TTCGACTCAG CCAGTCTCAC TGGGGCCTTC 600
AAATCACAGG GGCACCCACA TAAGGAGTCA ACTGGCCTCT GACAAAGCAG CAGAGGGATG 660
CAATGGTGCA AAGGCATTTT CCTCAATAAA CGCTGCTGGA ACAACTGGAC ATCCTCATGA 720
AAGAGAATAA ATCTAGACCA GACCGTATAC CCTCCACGAA CATAAATTCA AAATGAATCA 780
CAGGCCTGGC ACGGTGGCTC ACGCCTGTAA TCCCAGCTTT CAAGGAGGCA GAGGCAGGAG 840
GATTGCTTGA GCCCAGGAGC TCGAGACCTG CCTGGGCAAT ATAGTGAGAC CCCGTTCTCC 900
ACAAAAAGTG GGGGAAAAAA AAGACAAAAT GAATCACAGA CCCAAATGTA AAATGCAAAA 960
CTATGCAACT CCTAGACAGT AACACAGGAG AAAACTTAGA TCACCTGGGG TTTGGCAGAC 1020
TGTTTAGATA CAAAACCAAA GGCACAGCCC ATGAGAGAAT TGATTAAGAT GGACTTCACG 1080
AAAATAATAA CTTTGTGCTT TGTGAGAGAC ACTGTCAAGA GAAGGAAAGG ACAGCCGGAC 1140
GTGGTGGCTC ATGCCTGTGA GCCCAGCACT TTTGGAAGCC ATTTGGCGGG ATGGATCCCT 1200
TGAGGCCAGG TGTTTGAGAC CAGCCTGAGT AACAATAGTG AGACCCCATC TCTACAAAAA 1260
ATGTAAAAAT TAGCCAGGGA TAGTGGCACG CACCTGTAGT CCTAGCTACT CCAGAGGCTG 1320
AGGCAGGAGG ATCACTTGAA CCCAGGAGTT TAAGGCTGCA GTAAGCTGTG ATCATGCCAC 1380
AACATTCCAG CCTGGGCAAC AGAGCAAGAC ATTTCTCCTA AAAAAAAATA AGGCCAGGCA 1440
GGGTGGCTCA TGCCTCTAAT 1460
|
