| Tag | Content |
|---|
EnhancerAtlas ID | HS062-03464 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr12:4966420-4967900 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:4967051-4967070 | CTGCCACTAGGGGGAACCA | + | 7.1 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 2 | ID | Chromosome | Start | End |
| GH12I004857 | chr12 | 4966767 | 4967410 | | GH12I004858 | chr12 | 4967701 | 4967850 |
| Enhancer Sequence | CATGTGCCAC CACGCCCGGC TAATTTTATA TTTTTAGTAG AGATGGGGTT TCTCCATGTT 60
GGTCAGGCTG GTCTCAAACT CTTGACCTCA GGTGATCTGC CTGCCTCGGC CTCCCAAAGT 120
GCTGGGATAA CAGGTGTGAG CCACTGTGCC CAGCTGTTTC TGGTTATTAA TAGGAACAAA 180
ATACCAGGGC ATGCTTTGTC TAGGTCAGTC CTCATTCTTC ATTGTGGATC AGAATCAGCT 240
GGAGAACTTG TCAAAATGCA GATTCCTGGG CTCTGAACCC CCGAGTTATG GACTCAGTAG 300
GCGTAAGAGG CCTGAGAATT TGCATTTCTA TCCAGCTCCC AGGTGATGCT GATGCATAGG 360
TCAAGGACCA CACTTTGAGA AGCACCGGCG GGGAACACAG TGTTACCAGG TCTTGGTCTC 420
CATCCAATGC AGTAAACACT ATGCGATAAC AACCTGGGGG CTTTTGAGCT TACAGGAACA 480
GTCAATGCAA TAGAAGCACG CGCTGCTAGG TCTCCAAGGA AACAGGGACA GTCTCTTCTC 540
CCGCTGTTAG TTAATGAGAG TGTGGTTGTA ACTAAACTAC TGGCTAATTA CCACGATCGT 600
GGGAAGTGTC CCAGGTCGGC GCTATGAGCT TCTGCCACTA GGGGGAACCA GGGCTATTTC 660
TCTGCAGGCT CCAGGCTGTG AGAAGAGGAA AAGTACTGAA GAGAGCGAGC AAAGCCTTTC 720
AGAAAATACT GCAACACTGC GTGCCCGAGG CCCCCGCACA TCGCTGCAAT CTTGATGTGC 780
ACAGACACCG TCGAGAACCA AGGCTTGGCA GGGAGGGGGG ATGGTTGATT TTCTAAGTTG 840
TTTGGTTTTC CTCCCTTTCC TTAAAGTACA TCCACATTAA GCCGTTTATG CCGCGGGTGA 900
CCTGTAGTAT GAGAAGAAAC ACAGGTCGCT CTCCTGGCTT TGCAGATAGA GTAAGCTCAG 960
GAGAGAGGGA AAGGAGCTGG GCAAAATGCC AGCAAGGGAG GGCTGGGCTG GCGGGACCCA 1020
GATGTTCCCT GCCCAGGAGC GTCGTGGAGA GAAGGGGAGG CATGCCTGGG GTTTGGACTG 1080
GCCAGCTTGC AGGTGGCTGT CAACCCTGAA TGTTGTGGCA TAGGTCAGGA TGAGGTCCCT 1140
TGGGGTGGGG GAGGCAGAGT AATTCCTAAG GGAGAAAAAG ACAGGAAAGC AGGTTTTGGG 1200
GCTAAGAAGA CAAAAATGAC TGAGAGGTTA TTTTACCTGC CTTGAACTTG CAAACAAGTA 1260
TGGGTCATGA CCTCTTGTGA GTGCTGCCGC ATGCCCTGTC AGCTGCTGTC TTCTGGGGAC 1320
ACGCATATTC TGACCGCCAC AGAGGGCAGC ATAACAGCCA CAGTGCCTGC TGAGCAGGAA 1380
CGTGCCGCCT AACCGGTCCG TGGCGTCCCT GCCTCTTTCT CCCTCATTAA GCCTCTTTCC 1440
CAGGACCACA GCTTTGGAAA CAGCTTAATC TCTAACAAGT 1480
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