| Tag | Content |
|---|
EnhancerAtlas ID | HS062-04391 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr13:21068800-21070420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TBX20 | MA0689.1 | chr13:21069911-21069922 | TTTCACACCTA | - | 6.14 | | TBX2 | MA0688.1 | chr13:21069911-21069922 | TTTCACACCTA | - | 6.32 |
|
| | 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 |
| GH13I020494 | chr13 | 21069056 | 21070906 |
|
Enhancer Sequence | TTTTTCCCAA AAGTACTGCA TGAGATTAGA CAGATAATGG GAGAACAGGA GTCTCTTGTT 60
CCTCGATCCT CCAGGGACCA CCCCGGAATG AGAATGTCCC ATGGAGACAG CAAGCAGTGG 120
CAAGAAAAGA CACAACCACT CGCCTCTTTC AGAGCAGACT CAGGCTGAGG AATGTGCAGT 180
GGTGGTTCTG CCTCAGGCCC TTCCTCCCTG GGCAGCACAC ACAGGTAGGA CAGAGAACCT 240
GGGCATGAGG GAGAGACACG GTCACACATG AACCCATCAG CCAACTGCAA ACTCCAGGAC 300
CCTGCTGTGT GGTCCCGAGG GACGTCCAGT GAAAGCTGCG GAGGAGCTTC CGACATCTGC 360
AGACAGACCC CTGTGTTCTC TTTAGGGCCA ACAAATCCAC ATGCCACAAA TCAAACCCAG 420
CCTTTTGGCA ACATTTTGTC CCAGTTAGAT TAATTCCAAT TTTTTTTATT CTTTTGGAAG 480
AACTTCTGCA TCAAGCTTTG TAGAAGACGT ACATAAACAC CTAGAAAAGA TGTGCCAATC 540
AACCGGGATT TTCAAATGCC ACACACATAC CAGGCTGTGG CATTGCCACA CTTAACAGTT 600
AACGTCAGGT TAGAGGCACT AGTAGAAGGC TGCAATGTGC CAGTTCTACC TCTAGAGGTC 660
AGCCTAACAC TAGGACTCAA AATACTGGCT CCTAACCAGT AAAGTTAAAT TTTTACTTAA 720
AATTAGAGAA AAGGAAATGT TAACAATTCT CACGGTAGGA CAGGGTATGG GTGATTTTAA 780
TTTTTTTTAA TGTTTCTATC TTTGAAATGT ACTCAAAAGG AGCATGTATT TATTTTTAAA 840
AAAGACTGAA GAAATTGGAA CCTTGTGCAC TGATGATGGG AATGTGGAAA CGGCACAGCT 900
GCTGTGGAAA ACGTATGGTG GTAACTCAAA AAGTTAAAAA TAGAGCCACC ATATGATCCA 960
GGAACCCCAC TGCTGTGCAT ATATCCAAAA GAACTGAAGC GGGATCGCAA AGAGAGATTT 1020
GCACAGTCAT GTTCCTAGCA GTGTTGTCAA CAACAGAAGA AGCAAGCAAT CCAAAAGTCC 1080
ACCAACAGAT GGAGGGATAA ACAAAACATG GTTTCACACC TACGGTGGAA TCTTATTCGG 1140
CCCCACAGGG GAAGGAAGTC CTGTCATATG TCATATGCCA GGCTGGAGTG CAGTGGCGCA 1200
GTCTCAGCTC ACTACAACCT CCCCCTCCCG GCTTCAGGCG ATTCTCCTGC CTCAGCTTCC 1260
CAAATAGCTG GGACTACAGG AATGCACCAC CACACCCAAC TGATTTTTGT ATTTTTTAGT 1320
GGAGACGGGT TTTCACTCTA TGTTGGCCAG GCTGGTCTTG AACTCCTAAC CTCAGGTGAT 1380
CCACCTGCCT TGGCCTCCCA AAGTGCTGGG ATTACAGGTG TGACCCACCT CGCCCGGCCT 1440
AGGATGAACT TTTTACTTAA CATTATGCTT AAGTGAAATA AGCCAGACAC AAAAGGACAG 1500
ATGCCATATG ACTCCACCTA CAACAGGTAC CCAGAGCAGT CAAACTCACA GTGACAGAAA 1560
GTAGAATGGT GGATGCCAGG GGCTGGCAGA GGCACAAAAG AAGAGTTGTT TAATGGGCAC 1620
|
