Tag | Content |
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EnhancerAtlas ID | HS060-29528 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr6:32364400-32365650 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr6:32365265-32365276 | ATGAGTCATCC | - | 6.62 | Foxd3 | MA0041.1 | chr6:32364753-32364765 | AAACAAACAAAC | - | 6.32 | JUN(var.2) | MA0489.1 | chr6:32365265-32365279 | ATGAGTCATCCTTT | - | 7.08 | JUNB | MA0490.1 | chr6:32365265-32365276 | ATGAGTCATCC | - | 6.62 | Nr2f6(var.2) | MA0728.1 | chr6:32364541-32364556 | GAGGTCAGGAGTTCA | + | 6.22 |
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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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Enhancer Sequence | TACCTGCTTC TACCTGTATT TTTTTCAGTT TACAGACCAA TAATAAAATA ATTTTGCAAT 60 TAAAACTCCC AGATAGGCTG GGTGTGGTGG CTCAAGTCTA TAATCCCAGC ACTTTGGGAG 120 GCCGAAGCGG GTGGATCACC AGAGGTCAGG AGTTCAAGAC CAGCCTGGCC AACATGGTGA 180 AACCCCGTCT CTACAGAAAT ACAAAAATTA GTCGGGCATG ATGGTGGGTG CCTGTAATCC 240 CAGCTACTCA GGAGGCTGAG GTGGAAAAAT TGCTCGAACC CGGGAGGCAG AGGTTGCAGT 300 GAGCTGAGAT CATGCCACTG CACTCCAGGC TGGGTGACAA AGCGAGACTT TAAAAACAAA 360 CAAACAAAAA ACACCCAGAA TAAAGTGAAC AGTTTATAAA TTTGGCCCCA GATGCCTCTG 420 TACCTGACTC CTTATGTAAC AAACTGCAAT TTAACTTAGT ACGTCAACTA CTGAAAGCCT 480 AACTTAGGTT GCAGTTTGTT ACATAAGCAC TCAGGTACAG AGGCATCCTG GGGCCAAATT 540 TATAAATTGC TCATTTTATT CTGAGAGTTT TAATTGCAAA ATTATTTTAT GAATAAGCCT 600 AACTTAGGAG CTAAGGCTAA CTTAGGAGTA CACTTTTGTA ATAAATAGCT GAGTAGCAGC 660 TGCTGCACTT CTGTTAGTTG CAGGCAGCCA ACTGTTGAAA CCCTGTTCAA ATCGGCAAAC 720 GCCAGGCTGC AACCAATAGA GCTGTCTCTG TACCTCACTT CTGTTTTCTG TACCTCATTT 780 CCATTTTCTG TCCATAAATG CTGTCTGACC AAATTGCTGC TTTGAATTCT CTGAAACCGT 840 TCTGATTCTG AGGGATGGCT TGTTTATGAG TCATCCTTTT CTCAGTTAGA CTCTGCTAAA 900 TTTAGTCTGT CTAAAGTTTT TCTTCTAACA CTTCAATTCT GTATGATTTT AAACTACTTC 960 TTAATCTGTC TTAAACTACT TCTTAATGCC TCAGTTTCTT AAACTGTAAA TTTGCTATAC 1020 AACTACCAAA ATCATAATGT TTCAGAGTTG AACAAAATAG TTTGCATTAA GTGCCTGGAA 1080 GACCCTGCAG CGTGAGCAGA GGTGCACAGA CCTGTGAGAC TTGAAGGCGT TGGAGCCATC 1140 CCCACCCTCT GACGTGGTAA TAGGGAGGGG TTTAAAAACA TGTCTCATGT GGACTTTTGG 1200 TAATGATATT TGAAGAAGCT TTCCTCTAGG TGGACTTTAT AGTACCTTGT 1250
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