| Tag | Content |
|---|
EnhancerAtlas ID | HS052-34230 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr6:170712530-170713630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TBX21 | MA0690.1 | chr6:170712959-170712969 | TTCACACCTT | - | 6.02 | | TBX2 | MA0688.1 | chr6:170712958-170712969 | TTTCACACCTT | - | 6.62 |
|
| | 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 |
| GH06I170402 | chr6 | 170711584 | 170715999 |
|
Enhancer Sequence | ATTTCTTGTG TTAGTAAAAA AACTAAAAAT GCCTCTTCAT GAAAGTATTC AGTCACTGCC 60
AAAAGTTGTC AAGTTTCTGG AGCCTGAGTG TGTGGACAGG TAGGGGGTCC TGGGGAGCCT 120
GGCCTGAACT CTCTGGTCCA CTTCAAAGGC CTCAGAGCTC AGTGCAGGCA GCTGCCCCGA 180
GAACAAAGGC TGCTCAAGTG AGAAGGCTTT AACCTCTTCC TTGCTGTTGC TCAGCCCCGC 240
TGGAAAGAGA TGACGTGTTA AATTCCACAG TCCATAGCTA CAATTTGCCT GTGATTTTCC 300
AGATTGTCAC TTCTCTGTGG TGATTCTGTA GGAGGCCTGC CATAAAACTG CTGTGATCAT 360
CTGTGGTAAC AAGGGTGGGG GCAGAGTAAC AAGGGTCTGG AAACCTCACT TTGGCTGTAG 420
CCCTCTCCTT TCACACCTTC TGCCGGAGCC CACACTTTTG GGGGAGGGGA GAGACCCAGG 480
CTGCCCACGG CAGGAGTGGG TCAGAGGAGA GGCATGGAGA CCATCCCCAG TCACGGCAAG 540
TGAAGGCTCT TGCCGTCATA CACCAGAAGA TAACTCAGAG CAGGGAACTC TGGAAGAAAA 600
GTGTTATTTT TAAAATGTGA AAAACTGTCA CCGTTTTTGC TACTAGTAGG GAGGTTCTGC 660
CCCGAGTCTC TTCCCAACGT TCCCTGTCTA TCAGAAAGGC AGACAGTAGC CACCCAGGCT 720
GGGCCAGCCG CAGAAAGAGC TGCACGTGGG CTTTTCTGTG TTGGCAGAAC GTCCATGGTG 780
AGCCATCTGC ATGTGAATTT CCATTTCCAA AAGTCGTCAG CAATAGTAAA TGCCTAGAAA 840
TCACGCAGAT GGATGGAGCT GGTGTGAAGA GGAACAACTT TGACATTGTT TCCTTCCACG 900
AACCTCTTAA TTAATTGCTT CCACTTTAAT GGAATAATTA TGGAACACAG TTTTAATGGC 960
ATGTGGCCAC AACTGTAAAG AGGATAAAGC TGTGTCCTCC AAATACAGCT CAGCATCTTT 1020
GTTCATACTT AGAAATGTGC AGCATTCTTG TTTGTGTATT GAGAGAGATT TAATTCTTAC 1080
TTTGGTTTTC ATGTCTGTTT 1100
|
