Tag | Content |
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EnhancerAtlas ID | HS187-26058 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chrX:153554820-153555930 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF3 | MA0522.2 | chrX:153554910-153554920 | AGCAGGTGTT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH0XI154325 | chrX | 153554337 | 153556315 |
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Enhancer Sequence | AGCAGGTAAC ATCCAATTTG GTTGCTAAGG ACTAGGCTGC TCCAGAATTC ACAGTTGCAA 60 GTACTCAGAA TGGCCAGAGT GCTGCCATAA AGCAGGTGTT TCCAGAACTG TCCACTGTGT 120 GCCATAACGT AGCTGGAAAA CGCCACCAAA TGGAAAAGTT AGTGTTCACC TTTGGTGTTA 180 ACTACAGGTT CTGTTTCTAT GGGGAGGGTC TCTTGACATT CACATGGTTT GCAGAGCTTG 240 CTTATTTCTG TCGTCTCTTT TCTAATAATT TTCCTGTCCT GACAAAAGCA AGTAAATTTA 300 CTGATAGTAA AGGATGTGAG ATAAATGTGT GTGATAACAT GCATGGCATG GATCGTTAAA 360 GGGCTGGGCT TTGAAAAGAG GACATGGATA TGTGTGCATG CGTGTATAAG TATTTTAAGA 420 GGCCAGGACA TCCTTAAAGA ATGGGGTGGC TCAGAAACCC TTTCTGTACT ATCAGCAATG 480 GTTCTTAAGC TACAGGGAAA CCTATACAGA GGGGAAGTGG AGAATAATTC CAGATGCCTC 540 CGATGGGTAG CTTTGGAGGC AACAATCTAT GAAAGAAGCC CAGGAACTCT GTCTTTGCTT 600 GCAGAATAGT ACGTTGTCGA GAGCGAGGGC TTTGATGTCA GCCCCGCCTG GCTGTGGGTC 660 CCAGCCCTGC CCTGGGCCAC TTCCTCCTGC TCTGAGATTT GCTTTCCTCA GCTGCAGAAC 720 GGTTGTGCCA CTGAACAGAT CTTACAGGGA GGCTGTGAGG GTTCTCAGAG TTCAGGCACA 780 CAAGATCTTA GCACTCAGCG TGTTGCCAAT GCCCAGAATG TTCTCATTAA CATGTTAGTC 840 ACTGGAGTCC AATCTTTGCA TGCCATAGTG AGCTCTCAAA CCAGACTCCT GATGGGTATG 900 TGGCGTATCC ATGCTCCAGG ACAGCTGGAG CAGTGTAATT TCCTATCAAA AAGTATGTGT 960 CCTGGCTTGT AAATGCATCT GATTTTTTTA GTAGTGAGTT ATTAAGGAGT GAAATTGTTA 1020 GAATTGGGGG ATAGCGGCAT AGCAAAGTGC CTTCCACTTT GACATGCATT CTGTGTGTAG 1080 TAACCACGGC ATTCTGTTTT GCTGGCACTA 1110
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