Tag | Content |
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EnhancerAtlas ID | HS051-22442 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr5:148818750-148820480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr5:148819532-148819543 | GGGTGACTCAG | + | 6.02 | JUNB | MA0490.1 | chr5:148819532-148819543 | GGGTGACTCAG | + | 6.02 | LMX1B | MA0703.2 | chr5:148819259-148819270 | TTAATTAAATT | - | 6.32 | Lhx3 | MA0135.1 | chr5:148819248-148819261 | TAATTAATTAATT | + | 6.78 | Lhx3 | MA0135.1 | chr5:148819252-148819265 | TAATTAATTAATT | + | 6.78 | Lhx3 | MA0135.1 | chr5:148819245-148819258 | AATTAATTAATTA | - | 6.78 | Lhx3 | MA0135.1 | chr5:148819249-148819262 | AATTAATTAATTA | - | 6.78 | Lhx3 | MA0135.1 | chr5:148819253-148819266 | AATTAATTAATTA | - | 6.78 | Lhx3 | MA0135.1 | chr5:148819244-148819257 | AAATTAATTAATT | + | 6.92 | Lhx3 | MA0135.1 | chr5:148819256-148819269 | TAATTAATTAAAT | + | 6 | NFE2L1 | MA0089.2 | chr5:148819532-148819547 | GGGTGACTCAGCAGC | + | 6.1 | Nfe2l2 | MA0150.2 | chr5:148819530-148819545 | GAGGGTGACTCAGCA | + | 6.74 | PHOX2A | MA0713.1 | chr5:148819260-148819271 | TAATTAAATTA | - | 6.62 | POU6F1 | MA0628.1 | chr5:148819246-148819256 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr5:148819250-148819260 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr5:148819254-148819264 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr5:148819246-148819256 | ATTAATTAAT | - | 6.02 | POU6F1 | MA0628.1 | chr5:148819250-148819260 | ATTAATTAAT | - | 6.02 | POU6F1 | MA0628.1 | chr5:148819254-148819264 | ATTAATTAAT | - | 6.02 | PROP1 | MA0715.1 | chr5:148819260-148819271 | TAATTAAATTA | + | 6.32 | PROP1 | MA0715.1 | chr5:148819260-148819271 | TAATTAAATTA | - | 6.62 | Phox2b | MA0681.1 | chr5:148819260-148819271 | TAATTAAATTA | - | 6.62 | TFAP2A | MA0003.3 | chr5:148820053-148820064 | AGCCTCAGGCA | + | 6.32 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_23396 | chr5:148819274-148820362 | Colon_Crypt_1 | SE_24335 | chr5:148819616-148820345 | Colon_Crypt_2 | SE_40559 | chr5:148819120-148820087 | K562 | SE_47454 | chr5:148819269-148820363 | Panc1 | SE_50445 | chr5:148819404-148820370 | Sigmoid_Colon |
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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 |
GH05I149438 | chr5 | 148817851 | 148828080 |
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Enhancer Sequence | CTATTGGGAG TTGTACGCTG GTGTCTTGGC CTTTGTGTCT ATAATCATTA ACGCCTCCCC 60 CCACCTTTAC GCCCACTTGT AGATACAAAT GCATATAAAA CATTCAAGCA TATACCTACA 120 AAGCTGTTAA CAGTGGTTAG TTCTGAGATG GTGGTGAGAG GCTACCCATT ACACAGTTCT 180 GCCTCACTTT AAATTATCTT CAAAGGACTG GGCACAGTGG CTCAGGTCTG TAATCCTAGC 240 ACTTTGGGAG GCCAAGGTGG GCAGATCACC TGAGGTCAGG AGTTCGAGAC CCGCTTGGCC 300 AACAGGGCAA AACCCCTTCT CTACTAAAAA TACAAAAATT AGCTGGCTAT GGCAACGCAC 360 ACCTGTAATC CCAGCTACTT TGGAGGCTGA GGCAGAAGAA TCACTTGAAC CCAGGAGATG 420 GAGGTTGCAG TGAGCTGAGA TCGTGCCACT GCACTCCAGT CTGGGCAACA GAGTGAGACT 480 CCATCTCAAA AAATAAATTA ATTAATTAAT TAATTAAATT AAATTAAATT ATCTTCAAGG 540 AATCTGCTTC TCTAATTAGT AAATAGACAT CTGTTCATCC AGAGAAAAAT CTGGAAGAAC 600 ATACACCAAA ATGTCAACTG TGGTTCCATC TGGGGAGCAT AAGCATGGGA AACGAGCTAC 660 CTTCCACACT GTATATTTTG ATGTTGTTTG AACTTTATAC GATGAGCATG TGCCACTTTT 720 GTAAGCAGAA AAAGTAATTA AGACCTTTTT TTTTTTTAAC GTAAAAGGAA GAATAAAGAG 780 GAGGGTGACT CAGCAGCTGG CAACAGAGGC CCCACCTTCC TTCCTGTGCT CCTTTCCACC 840 TCTCCCCACC CACATGCACA CACCCTAACT GGAAAAACCT GGGCTCCTGC CGGCTGCGTC 900 TGTCCTTCCC GTCTCTCCTC CTAGTGGTTG AACTGGGCCA CCGCTAATCC CAGGGCAATA 960 ATATCTCCCC CTCACCTTTA TTAGTGGCTT GTGGTTTATG GGATGCCTCC AGTGCCAGCT 1020 CATGTTTAAT CCTCCCCATG ATGCTGTGAG GTAGCTATTC TCATGCCCAT TCTACAGACA 1080 TGGAAACTGA GGCTCAGCAA AGCTAAGCTC CCTGCCAGAG GTCACATAGC ATGTCTGCGA 1140 TTGTGCCTGG GCCCAAATTC CCAGGCCAGG CTTCTTGAAT GCTGCATCAG TTCAAGCTCA 1200 TTTCAGGAAC CTGAGGTTTG CTACCTAAAA TCGGCCTGTT GGATCTTGTT CAGCCACATG 1260 AAACAGCAGA TGTGCGCCTG TTCTCTGAAG AGCCCATCCC TGCAGCCTCA GGCACTCAGC 1320 CCTTCCCTGC ACTGCCTTGG CCCTGGGGCT GAGCCTGAGA GAGAGGAATG GAAGGGCGCT 1380 TTGGGTCCTG ACAGAGAAGC GTGGGTAAAA GGGAGACAAA AAGGGGGCAG ACCCCTAGCA 1440 TACACACAGA TGGGCACAGG CAGGCAAACC CTACAGTCTA GGAAAGTGGG TAGGGGCCAG 1500 GCAAGGTGGC TTACGCCTGT AATCCCAGCA CTTTAGGCCG AGGTGGGAGG ATCACCTGAG 1560 GTCAGGAGTT TGAGACCAGC CCAGCTAACA CGGTGAAACC CTGTCTCTAC TAAAAATACA 1620 AAAATTAGCC AGGTGTAGTG GCGAGCACCT GTATTCCCAG CTGCTTGGGA GGCTGAGGCA 1680 AGAGAATTGC TTGAACCCGG CAGGCAGAGG TTGCAGTGAG CCGAGACCAT 1730
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