Tag | Content |
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EnhancerAtlas ID | HS187-21879 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:139305240-139306670 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr6:139305895-139305909 | ATGAGTCATTTCTC | - | 6.84 | NFIA | MA0670.1 | chr6:139306434-139306444 | ACTTGGCACC | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65081 | chr6:139305391-139309046 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 139305368 | 139305421 | chr6 | 139305536 | 139306146 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I138984 | chr6 | 139305581 | 139305730 |
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Enhancer Sequence | GCGTCTTGCT CTGTCATCTA GGCTGGAGTG CAGTGGCGCG ATCTTGGCTC ACTGCAACCT 60 CCTCCTCCTC CCAGGTTCTA AGTGATTCTC CTGCCTCAGC CTCTGGAGTA GCTGGGATTA 120 CAGGCATGCG CCACCACATG CGGCTAATTT TGTATTTTTA GTACAGAAAG GGTTTCACCA 180 TGTTGGCCAG GTTGGTCTCC AACTCCTGAC CTCAGGTGAT CCACCTGCCT CAGCCTCCCA 240 AAGTGCTGGG ATTACAGGCA TGAGCCACTG TGCCCGGCCC ATATCTGATT TTTTGTCCCA 300 CTCCCACCAC TATAGTCCAG GTTAGGGTTT CTCAGTCTCA GCACTATTGA CATCTTGGGC 360 ACATAATGCT TGTGGAGGCT GTCCTGTGCA CTGCAGGATG TTTAGCAACA TTTCTGGCCT 420 CTACCCACTA GATGCCAGTA GAACTGCTCT CTCCCCTCTA GTTATGACAA TCAAAATGTC 480 TCTAGACACT GCCAAATGCC TCTTCCCCAT TGTCACCTTC ATTCCCATGT TTGAGTACCA 540 CTGGCCCAGT TTCTCACTTC GTATCTGCCA TACAAAATCA GCCCCCAAGT TAAGTCTACA 600 GTTTTATTCC TCTAATTCCT GTGGCCCTGA CAAACGACTC CTAAAGCACT GCTTTATGAG 660 TCATTTCTCT TAAATCTACC ACTCCCTGTT ACCTACACAA TTAGTTCAAA GCTCTCCATC 720 CAACCTTGAT AATCTGGCCT CAATTAAACA TTATTCCACA AAGCACCTCA TATAGTGGCT 780 ACCCAGCAGT CCTTCAATAA CATATCCAGT CTCTCCCTTT CTATTCTACT GCTGTCACCC 840 TGGTTGGATG TCCATGACCT AGCACCCAAT CCAGACCACT GAAAGAGTGT CATTCCTTAC 900 CCTTTCTGCC ACTCAAAGTC AAAAACTTTT CAATGGGTCT CCATTGCTTG CTGAAATATC 960 GTTATCTGCT GCCCTTCTTC AGAGTCTTTC CCAATATGGC CTCTTTCTAA TTTTATATTC 1020 TGTTATCCCG AAAACACTAG TCCTTGAAAA GGCTCCTACA CTTTCCACTT CTGATCACTT 1080 TTCTCTGCCT GGAAGCCCTC ATAATTCCAT TCCCCTCACT CCACCCTAAT TTAAAGTCCA 1140 TCTGAATTAA GTCAAAAAGC CTTTCTTGGT CATACCTCCT TAGCATTTCA TAACACTTGG 1200 CACCTCTCCT ATGGCATACA TTATACCTTA TGTTATACAT GAGCACTCCT ATAATTGACA 1260 AGATCCTCAA GAGCTTCTTA CTCCTCTTCT GATGCCTGCA ATGCCTAGCC CAGTGTTAAG 1320 TAGAGAACTA AGCATTAGAT ATGAGCTGCC CCAAATGTTT CCCACTTAGA AAGCAATGGA 1380 GGACTGTGTT TTCAGACAAT CCCAAACTCC CTTAAGGGAA TTAAGCACAT 1430
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