| Tag | Content |
|---|
EnhancerAtlas ID | HS187-11021 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:75779780-75781680 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxo1 | MA0480.1 | chr17:75780367-75780378 | TCTTGTTTACA | + | 6.02 | | PHOX2A | MA0713.1 | chr17:75781626-75781637 | TAATTGGATTA | - | 6.02 | | Phox2b | MA0681.1 | chr17:75781626-75781637 | TAATTGGATTA | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_33469 | chr17:75773608-75780941 | H2171 |
|
| | 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 |
| GH17I077783 | chr17 | 75779614 | 75781610 |
|
Enhancer Sequence | TTCCGGACAG CAGTCGTTCT TGCTAAGAAT TTCTAGAGTA GGAAGCAAGG GTCTTGCTCC 60
CTGCCCACTG TGCAAATGAA AGAATCAAGT ACAAGGAGTG AGAAAGACAG CCTAATGTTT 120
CCTGGACATG GTGGCTGGGG ACTGGCTGGA AGTTGGGGAG GGGACCCCCC CCAGCCTAGG 180
TAGGCCCAGG TTCCTGCAGC CACAGCCTTG ATGGTGATGG TCCAGGGAGA ATGGCTGAGG 240
GTGCCCACCT GGCAGGACCA CAACTGTGAT GAGTGAAATC AGCACGAGAA GGACTCTGGC 300
ACCCAGTTTG GGGGTGGGCA GGCAGGATGA GGCAGTGATG GACACGCGCA GCCCCCACCA 360
CACCTGCCTT CATCAGGGGC CTCCGGGTGC CCGGACGGAT GCTGGTGACC ATGGCAAGGG 420
AGGGCTCAAC GGTGCTGCCA CAGCGGTGGT GCCTCTCGAG AGGCAGCTGG TTAGAAGTGA 480
GAACGCAGTG TCTTCCGCCT CTCCACACCT TCTCAAGGAG GTGATTTCCC AGCCACCCGC 540
GAGCAGCCGA GCATCCTCAT TCAGCTCCTC AGGTGTCAGG GCACTGCTCT TGTTTACACT 600
GTCATCGCCC TTGCACTGAA CAGCAGAGGC GTGGACTCCT TTTGGCTGAT CTTTGCTCTG 660
AGCACCCAGC GCTATGCCAA GGATGGGGAG CCCCATCCAG AGCCCAGGCA CCATCTCCAA 720
GCAGATGGAG GAGCTAGGAA CAGCTAGGAG GGTCTGTTAC CAAAACAAAA CTGGCTCCAC 780
TCACCCAGGT TGGTAAAGCC AAATACCCAC ACTGAGGTTT GCAGCAGGAG AAAGGAGGGC 840
GTTTATTTGC CAGGTGCCAA GCAAGGAGAA TCAGGCAGCT CACACTTAAG ACCCAACATC 900
CTCAATGGCT CACGAGCAAC GGTTTTGTTT TTTCTTGTTG GTGGTTTCTT TTCTTGTTGT 960
GTCTCACTCT GTCACCCAGG CTGGAGTTCA GTGGTGAGAT CACGGTGCAC TGCAACTTCT 1020
GCCTCTTGGG TTAAAGCAAT TCTCCTGCCT CAGCCTCCTA AGTAGCTCAG ACTACAGGCA 1080
TGCACCACCA TGCCTAGCTA ATTTTTGTAT TTTTTATAGA GTTGGGGTTT GGCCTTGTTG 1140
GCCAGGCTGA TCTCAAACTC CTGACCTCAG TTGATCCGCC CACCTGGGCT TCCCAGAGTG 1200
CTGGGATTAC AGGCATGAGC CACCACACCC GGCCACAAGC AAGGGTTTTC AAAGGCGGGA 1260
GTATATTTCA GGAAAGCAGA AGTTTCAGGC AAAATCGTTA ATCAGTACAT GAACATTATA 1320
CATTGGTTTG GCCTCAAAAG GTGGGATATC TTGAAGTGAG GGGGCTTACA GGACCAGACG 1380
GGCAGAGAAA AGTCTCATCC GTCCCCCAAC CCCCATCCTC AGAACTGGCC TGGCTTGCAA 1440
GGAGGGGATT TTGTCTCCAT TTCACAGATA TTAAGGAAAT TGGGTGCAGA AACTTTCAAG 1500
AGCCTGCCCA GGATTCACAG AGTGAGAAGC CAGGGCAAAG CCAGAATTTA GACCTAGTGC 1560
TGTGTGGACT CACCCTTCCC ACAGGAACAT CCTGCTTCAG AACTGAACAC CTGCAACTCA 1620
GCGTGGCTCA CTCGATCCCA GCTCTAGGGG GTGACCCGGC CACCCACACC ACTCTCTCCC 1680
CACCCCACAC CATGGGTTCT GGGCTGCCTC ACCCTCCCTC ATTGCCTCCT GCGTGCACAG 1740
AACATCCTTT CCATGGGGGA CATGCATCAG GAGTAGAGAA GGCTGGGCAG GGACATGGTG 1800
TGGGATCGCA TGCGGCTGAT ATTCCTGTTA AATAAATACA TTTTGCTAAT TGGATTACTC 1860
AGACAGTATA ATATACTACT GGATTTCCAA CATGATGCTA 1900
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