| Tag | Content |
|---|
EnhancerAtlas ID | HS002-02852 | Organism | Homo sapiens | Tissue/cell | A375 | Coordinate | chr13:44578400-44579690 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr13:44579571-44579582 | TCTGATTGGCC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GATCTCAACT CACTGCAACC TCTGCCTCTC AGCTTCAAGT GATTCTCCTG CCTCAGCCTC 60
CTGAGGTAGT AGCTGGTAGT AGCTGGGATT ACAGGGGTGC ACCACCACAC CCGGCTAATT 120
TTTGTATTTT TAGTAGAGAC AGGATTTCGC CATGTTGGCC AGGATGGTCT CAAATGCCTG 180
GCCTCAAGTG ATCTGCCCAC CTTAGCCTTC CAAAGTGCTG GGATTACAGG CGTGAGCCAC 240
TGTGCCCAGC CCAGCTGGGT GATATCACCT CCTAACAGTG TCAATGCCAC AAGTCTTACT 300
GCCCCACTCT GCCCCTTTTG ACTTACTATT CTGGCTATAT TCATTTATCA TGACTTTATG 360
CCTTAGTTTC TGCTGTTTTC TCTGCCCTTG ATGCACTTCC ACTTGGAAGA TCCCAACTCA 420
AAATTGCTTC AAATCCTTAT TGGAACATAG TAAAACATGG TAAAATACAA AAACAAAATG 480
AAACAACACA AACAATCCAG CAACTAAAGT CTACTCATTC TCAGAATCAG GTTCATTCTC 540
AGAGACTTTC CTGATCCCTG GTGGTAGGGC AGGTGGCTTC TTCCTGGCGC CCCCACAGGA 600
CTGTGATCAC ACCCTGGCCA CTTCCCACAT AGGCTGAAAA GTTTGTTGAC TGTGGGAGGA 660
CAGGGACCAT ATCCTACTCA TCCTTCTGTC CCCCTTTCTA AACAGTCCAT TATCCAGAGG 720
GCCTGCTGTG TCCAGCTGAT CTGCAGTTGA CTACATATCC CCTGCACTGC TCTCCGGAGG 780
CTGACGCTGA TGACTCAGTG CCCAGAAGAG AAGGGCTTTT CCTGTATGAG CCACAGATTC 840
TCTTTAAATT GCCTTCAGGT CATGCACATT TGTTGCCATC TTCTTTCTTT ACTGTAAATT 900
ACCAGGATTC CTGGCTACTT TACCTTTATT TTCTCCAGGG TCTAGACTGC GTCTGATAGG 960
ATCATAGGTT CTTGCTCTCT GTGTGGTGTA GTAATTATAA ATTTTCTTGG TGAGCAGATT 1020
AAACATGTAG ATTCACGTTC AACTCTGGGG TTTTCCCCCA AGGATTATAA TTAATACCCT 1080
AGCAAACAGG GATATACGCA TCCCTGTTCA CATCTGGGGT ACAGAAAGAG CACCCCTTGC 1140
CTCAACAGGT AACCCGAACC ATTAGCTTTG CTCTGATTGG CCTCATTCAC CCCAAACCAA 1200
TCTGGATGGC TGGGTTCAAG CATGGAAATG TAGCCATCCA AGCTGTTGAT TCATCTGCAT 1260
GACTTAAAGG ACTTGAAATC TTTAACCAAA 1290
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