Tag | Content |
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EnhancerAtlas ID | HS047-27710 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr5:148818490-148820990 |
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 | CCTATGACTA ATCTTTCCCC GTAATTCTGC CTCCAAACCA AGCAGGAGTG TATGCATAGT 60 ATGATCCCAT TTTTGCAGGA GGAAAAGACT CTTTGTGTGG GCCTATAACA ATAGCTAATC 120 CTGGCTGAGC CAGACATTGT GCTGAGCTCA GCATACTTTA TCTCATTTCA TTTTCTCAGC 180 CACACTCTAA ACAAGGTGGA ATTCTCATCT TCCGAGGAAG AAAATGAGAC TCAGAGAGGT 240 CACTCGCCCA AACTAGTGAC CTATTGGGAG TTGTACGCTG GTGTCTTGGC CTTTGTGTCT 300 ATAATCATTA ACGCCTCCCC CCACCTTTAC GCCCACTTGT AGATACAAAT GCATATAAAA 360 CATTCAAGCA TATACCTACA AAGCTGTTAA CAGTGGTTAG TTCTGAGATG GTGGTGAGAG 420 GCTACCCATT ACACAGTTCT GCCTCACTTT AAATTATCTT CAAAGGACTG GGCACAGTGG 480 CTCAGGTCTG TAATCCTAGC ACTTTGGGAG GCCAAGGTGG GCAGATCACC TGAGGTCAGG 540 AGTTCGAGAC CCGCTTGGCC AACAGGGCAA AACCCCTTCT CTACTAAAAA TACAAAAATT 600 AGCTGGCTAT GGCAACGCAC ACCTGTAATC CCAGCTACTT TGGAGGCTGA GGCAGAAGAA 660 TCACTTGAAC CCAGGAGATG GAGGTTGCAG TGAGCTGAGA TCGTGCCACT GCACTCCAGT 720 CTGGGCAACA GAGTGAGACT CCATCTCAAA AAATAAATTA ATTAATTAAT TAATTAAATT 780 AAATTAAATT ATCTTCAAGG AATCTGCTTC TCTAATTAGT AAATAGACAT CTGTTCATCC 840 AGAGAAAAAT CTGGAAGAAC ATACACCAAA ATGTCAACTG TGGTTCCATC TGGGGAGCAT 900 AAGCATGGGA AACGAGCTAC CTTCCACACT GTATATTTTG ATGTTGTTTG AACTTTATAC 960 GATGAGCATG TGCCACTTTT GTAAGCAGAA AAAGTAATTA AGACCTTTTT TTTTTTTAAC 1020 GTAAAAGGAA GAATAAAGAG GAGGGTGACT CAGCAGCTGG CAACAGAGGC CCCACCTTCC 1080 TTCCTGTGCT CCTTTCCACC TCTCCCCACC CACATGCACA CACCCTAACT GGAAAAACCT 1140 GGGCTCCTGC CGGCTGCGTC TGTCCTTCCC GTCTCTCCTC CTAGTGGTTG AACTGGGCCA 1200 CCGCTAATCC CAGGGCAATA ATATCTCCCC CTCACCTTTA TTAGTGGCTT GTGGTTTATG 1260 GGATGCCTCC AGTGCCAGCT CATGTTTAAT CCTCCCCATG ATGCTGTGAG GTAGCTATTC 1320 TCATGCCCAT TCTACAGACA TGGAAACTGA GGCTCAGCAA AGCTAAGCTC CCTGCCAGAG 1380 GTCACATAGC ATGTCTGCGA TTGTGCCTGG GCCCAAATTC CCAGGCCAGG CTTCTTGAAT 1440 GCTGCATCAG TTCAAGCTCA TTTCAGGAAC CTGAGGTTTG CTACCTAAAA TCGGCCTGTT 1500 GGATCTTGTT CAGCCACATG AAACAGCAGA TGTGCGCCTG TTCTCTGAAG AGCCCATCCC 1560 TGCAGCCTCA GGCACTCAGC CCTTCCCTGC ACTGCCTTGG CCCTGGGGCT GAGCCTGAGA 1620 GAGAGGAATG GAAGGGCGCT TTGGGTCCTG ACAGAGAAGC GTGGGTAAAA GGGAGACAAA 1680 AAGGGGGCAG ACCCCTAGCA TACACACAGA TGGGCACAGG CAGGCAAACC CTACAGTCTA 1740 GGAAAGTGGG TAGGGGCCAG GCAAGGTGGC TTACGCCTGT AATCCCAGCA CTTTAGGCCG 1800 AGGTGGGAGG ATCACCTGAG GTCAGGAGTT TGAGACCAGC CCAGCTAACA CGGTGAAACC 1860 CTGTCTCTAC TAAAAATACA AAAATTAGCC AGGTGTAGTG GCGAGCACCT GTATTCCCAG 1920 CTGCTTGGGA GGCTGAGGCA AGAGAATTGC TTGAACCCGG CAGGCAGAGG TTGCAGTGAG 1980 CCGAGACCAT GCCGCTGCAC TCCAGCCTGG GCAACAAGAG TGAAACTCCA TCTCAAAAAA 2040 AAAAAAAAAA AAAGTGGGTA TGGGCTGGAT CAGAATCCTG GATATGGCTT TGATCAAATC 2100 ATTTAGTGTC TGTGGGCCTC AGTTCCCTCA TCTGGAAAAC GTGCATTACA GTAGCACCAC 2160 CTTATAGAGC AGTTCCAAGG ACTCAGTGGG GAATCCTTAG AGTGCATTTA GCACAATACC 2220 TGGACATAAT GCCTGCTGAA TAAGTGCTGC TTCTTGTTAT TAACAAGACT GAATTGATCT 2280 GATCAAAGCA GCTCCCTTTG GTTTCAGCGA ACATTTACTG AGTGCCTACT ATGTGCAGGC 2340 CTGGGGTAAG CCCTGGGGAT ATTGTGATAA AGTAGATGGA GCTCTGCTCT CACACAGCTC 2400 CCAAGCGATC AAGGGAGGCC AACCCAGAAA GAGGCAGACC ATTCCTGGAG GCCACCAGGG 2460 TGGAGGGGTC CATGTGAGGT GAGACCTTGA ATGCCAGACT 2500
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