| Tag | Content |
|---|
EnhancerAtlas ID | HS030-02950 | Organism | Homo sapiens | Tissue/cell | CyT49 | Coordinate | chr10:36262730-36264090 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr10:36262905-36262921 | ACTTAAGTAAACAAAC | + | 7.64 | | FOXP2 | MA0593.1 | chr10:36262909-36262920 | AAGTAAACAAA | + | 6.62 | | TFAP2C | MA0524.2 | chr10:36263882-36263894 | TGCCTTAGGGCA | + | 6.04 | | TFAP2C | MA0524.2 | chr10:36263882-36263894 | TGCCTTAGGGCA | - | 6.32 | | ZNF263 | MA0528.1 | chr10:36263378-36263399 | TTCTCCTTCCCTCCCACCTCA | - | 6.33 | | ZNF263 | MA0528.1 | chr10:36263401-36263422 | CCCTCCTGCCCTTCCTCTTCC | - | 7.25 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTCCATGACA CATGCAGTTT TTTAGAAGTC ATGGTGATTT ACAAGTAGAA GATTCTGCAT 60
TTGATGGGCC AGGGTTTCCT GGAGTTCTAA TCCAAGCCCT ATTCACTATA GATCAAGCCA 120
CTGTACCTCC TTTTCCAGAA GGGTAGGAAA CCCAAACTCA GTCTGATGCG GTTATACTTA 180
AGTAAACAAA CACACAACTT ACCTAGAGGC CCAGAACAAA TAACAAACAA TCGGGGAAGA 240
GGGCATGACC TCTCAGGTAG ATTACCTCCT CATTGTCATT TCTATTAGGG TAGAATGGCT 300
GATTTAACAG AAGGTCTGTC TCCACTGGGG ACTCCCTGGT TGTGCTGATG TTTGCTGTAG 360
TTACCAGCCT AATGGCTGCT TTGTAAGTTG TTTGGATTTG CTAATAATTC CTAATGAGGA 420
TAATTAAGCA AACAAAGCAA TGGGTAGAGA ATAGGGTGTG TAAATACGGA TACATTTAAT 480
GATGCACTGA CTGATGATTT CTGTTCCTTG GTTGTTAACT GTGAGAATCT ACCCCAAAGA 540
TGCTTGAGGT GTGAGCAGAC ACAGGGCGCT GCCACAGTTG CTTTTTCTGG ATCTCTGTAC 600
TATCCTCCCC TCCCTTAACA CCCCTTCCAC TCTCCTTTAC TTCTTTCTTT CTCCTTCCCT 660
CCCACCTCAC TCCCTCCTGC CCTTCCTCTT CCTCCCTGTG AGAGGACGAG TTAGGTCAGG 720
TCAATACATT GGCAGGGGTT TTAGGGAAAG GGTGGTTATT CTCCATGAAT CTAACCAATT 780
AGGCTTCTTG CATGGATGGA GAGTTTTAGG GGGTTGGTGG GTTAGAAAGC AGTGTGACTT 840
GGCAACTGCC AAGGGACTGG GGGACAAAAC CGCTGAGAGG ACTGCTGGTC TGGCTGGCAA 900
AGGCAGTGGA GTTGGGAGTC AAATATGGCG AGGTGACAGG ACAGGTCTGT GATAGACACC 960
CCCCCAGCAG AAGCAACTGG ACCCAGGTGA ATGGAGGCTG TTCTTTGGAA GCGATGAAAT 1020
GGAACTTTGG CAAAATGAAA TGATTTCAAT TTCAAGAACT TCACAGGGGA GTTTGGAAGG 1080
AAGCTCCTGT GATTAAGTGT GGGTTTGGGA AAGAATAGAG CAGAGTCCAG TCTGCGAAAA 1140
GAGCCACTGC AGTGCCTTAG GGCACTTCTA CAAACATGAA CCAAAAGGAC ACAGGAGTGC 1200
TGCCCAGACA GCAGGGGACA CGTCTGGTCA TGTGGGTTAC CTGAGCTTGT GTGTATGTGG 1260
GTCACAGTCA TCTGTATTTA ACATAGTGTA AATTAACACA GAGAAAAATG TGAAGGATCA 1320
GAATTTATAA GCACGTGTTC CATTAGTCAA AGGAGAAACG 1360
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