Tag | Content |
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EnhancerAtlas ID | HS187-17667 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr3:128744880-128746190 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIC | MA0161.2 | chr3:128745317-128745328 | TCTGCCAAGAA | - | 6.02 | ZIC3 | MA0697.1 | chr3:128746149-128746164 | GCGCTGCAGGGGGCC | - | 6.04 | ZIC4 | MA0751.1 | chr3:128746149-128746164 | GCGCTGCAGGGGGCC | - | 6.14 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_24388 | chr3:128745222-128746061 | Colon_Crypt_2 | SE_42689 | chr3:128743410-128746653 | Lung | SE_50819 | chr3:128743261-128746643 | Sigmoid_Colon | SE_53691 | chr3:128743406-128746612 | Spleen |
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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 |
GH03I129024 | chr3 | 128743793 | 128746643 |
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Enhancer Sequence | CTTAGTGCTT TGGTTTCCTC CTCTGTAAAT GGAGATAATG ACCTTACCTG TTATAGGGTT 60 TTCATGAGGA AGATGTTTGA AATATTGAGA ACAGCTTTCA GAACATTCTG AAGGGTTTAG 120 TTGGTATTGT CGTTGCTGTC CGTGCAGGAA GCTGTGCCTG GAGCAGGCTT TCTAAGACAC 180 ATGCAAGTGC TAGGAGGTGG AGTGTGGGGA TCCAGTCCAC CCCAGGCAGC CTGTGCCAGG 240 AAACATTTAA ACAGGCCCCT GGGGGTAAAA GCTGTCCCTC CATCTCATTT TGCTTGTTGA 300 AACCCTTAAA TGATTTAGGG AATAGAAGAA GCAGCAGCAT CTCATAGTGG AAAGATTTCA 360 ATATTAATGT CTAATTCAAC CTCCAACTGT ATTCACAATT CCAGCCGCTG AAGTCCCTTA 420 CCTGCTGACA TACCTCCTCT GCCAAGAAGC TCACTGCCTT CCACAGCACA TCCATCATTC 480 TTCATCAGCA GTTCCTGCGA GAAAGTTGTT CCTCCCAGTG AGCTAAAATC GCCTCCCTTT 540 GATTACCAAC TCCCATCTTT GCTGTCTCAC CCCAGTTAAA CACCTCCCTA TGGGGCCATA 600 TAACCAGGTA CCTGCCTCTA CCCTTGAGTC TTGGAGACAG TGACCTTATT CCCTTGTGTC 660 TTTTCTTCTC CAGGCTGTAG TCTGGAGCCT GTGGAGTAGG GAGATACTGG CACCTCCCCA 720 GTGAGATCTC AACTATTATG ACCTAAGCTG TAGTCACGCG GTCTCACATT GAAGCAAGAA 780 TCCCCACCCG GGGGTTTTCA CACTGGTTGC TGCTAAGCAA CGTGCCCATT CTCGGCTTGC 840 ACTGGGGGAC CCTGAATGCA GGATTTTATG AATCAGAGTC ATGGGCTCAA AAAACACGAA 900 ATTCCAGGGT TAGCCCTGGC TTTAGGCAAA GCCTGATCCA GCAGCTCAAC TGATGTTACT 960 AAGGGTCCTG TTTCTTTTGC CGTCATCTTT GGGCTCTATC TGCAGCCCCC AAGCATCTCC 1020 GGACGGCCCC CTCAGAGGCA CAACTTCCCG CTTCGTCGGT CATCATGCTC CGCGCCCTCA 1080 GGCAGTCAGC GAAACGCCGG AAACGCCTGC AGACGCCTGC AGACGCTCCT TGTGTTTCAT 1140 TGGCTACCCG TGCAGCCCTG GGCCACTCAC GGTGGCCAGG GTGGGGTTAT GCTGATGAGC 1200 ACGGGGAGGC CCCGCGGGCG GCGGCGGTGC TCGCAGCCGA GGTGCCGGCG GGGAGCTGGC 1260 CATGGGGAGG CGCTGCAGGG GGCCCCGGCG CCCGTGCCCC GTTTGGGCTG 1310
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