| Tag | Content |
|---|
EnhancerAtlas ID | HS069-02277 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr13:21068630-21070400 |
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 | ACACACAGGG TCTCTGGATG CCAAGGTCTG GGAACATAGT GAGTAACCAT TGCATCCTTT 60
AGGAAACTAT GTCTGAGCGC CTGATGTGCT CAAAGCACCT GCTCCAAGCC TTAGTAGGCC 120
AGCTGTGCGT CTTCAAACCT TTCCACTAAT CCAAAGCAAA CTTTTAGCCT TTTTTCCCAA 180
AAGTACTGCA TGAGATTAGA CAGATAATGG GAGAACAGGA GTCTCTTGTT CCTCGATCCT 240
CCAGGGACCA CCCCGGAATG AGAATGTCCC ATGGAGACAG CAAGCAGTGG CAAGAAAAGA 300
CACAACCACT CGCCTCTTTC AGAGCAGACT CAGGCTGAGG AATGTGCAGT GGTGGTTCTG 360
CCTCAGGCCC TTCCTCCCTG GGCAGCACAC ACAGGTAGGA CAGAGAACCT GGGCATGAGG 420
GAGAGACACG GTCACACATG AACCCATCAG CCAACTGCAA ACTCCAGGAC CCTGCTGTGT 480
GGTCCCGAGG GACGTCCAGT GAAAGCTGCG GAGGAGCTTC CGACATCTGC AGACAGACCC 540
CTGTGTTCTC TTTAGGGCCA ACAAATCCAC ATGCCACAAA TCAAACCCAG CCTTTTGGCA 600
ACATTTTGTC CCAGTTAGAT TAATTCCAAT TTTTTTTATT CTTTTGGAAG AACTTCTGCA 660
TCAAGCTTTG TAGAAGACGT ACATAAACAC CTAGAAAAGA TGTGCCAATC AACCGGGATT 720
TTCAAATGCC ACACACATAC CAGGCTGTGG CATTGCCACA CTTAACAGTT AACGTCAGGT 780
TAGAGGCACT AGTAGAAGGC TGCAATGTGC CAGTTCTACC TCTAGAGGTC AGCCTAACAC 840
TAGGACTCAA AATACTGGCT CCTAACCAGT AAAGTTAAAT TTTTACTTAA AATTAGAGAA 900
AAGGAAATGT TAACAATTCT CACGGTAGGA CAGGGTATGG GTGATTTTAA TTTTTTTTAA 960
TGTTTCTATC TTTGAAATGT ACTCAAAAGG AGCATGTATT TATTTTTAAA AAAGACTGAA 1020
GAAATTGGAA CCTTGTGCAC TGATGATGGG AATGTGGAAA CGGCACAGCT GCTGTGGAAA 1080
ACGTATGGTG GTAACTCAAA AAGTTAAAAA TAGAGCCACC ATATGATCCA GGAACCCCAC 1140
TGCTGTGCAT ATATCCAAAA GAACTGAAGC GGGATCGCAA AGAGAGATTT GCACAGTCAT 1200
GTTCCTAGCA GTGTTGTCAA CAACAGAAGA AGCAAGCAAT CCAAAAGTCC ACCAACAGAT 1260
GGAGGGATAA ACAAAACATG GTTTCACACC TACGGTGGAA TCTTATTCGG CCCCACAGGG 1320
GAAGGAAGTC CTGTCATATG TCATATGCCA GGCTGGAGTG CAGTGGCGCA GTCTCAGCTC 1380
ACTACAACCT CCCCCTCCCG GCTTCAGGCG ATTCTCCTGC CTCAGCTTCC CAAATAGCTG 1440
GGACTACAGG AATGCACCAC CACACCCAAC TGATTTTTGT ATTTTTTAGT GGAGACGGGT 1500
TTTCACTCTA TGTTGGCCAG GCTGGTCTTG AACTCCTAAC CTCAGGTGAT CCACCTGCCT 1560
TGGCCTCCCA AAGTGCTGGG ATTACAGGTG TGACCCACCT CGCCCGGCCT AGGATGAACT 1620
TTTTACTTAA CATTATGCTT AAGTGAAATA AGCCAGACAC AAAAGGACAG ATGCCATATG 1680
ACTCCACCTA CAACAGGTAC CCAGAGCAGT CAAACTCACA GTGACAGAAA GTAGAATGGT 1740
GGATGCCAGG GGCTGGCAGA GGCACAAAAG 1770
|
