Tag | Content |
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EnhancerAtlas ID | HS083-00788 |
Organism | Homo sapiens |
Tissue/cell | HCC1954 |
Coordinate | chr15:67340270-67342890 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr15:67342669-67342680 | CTGAGTCACCC | - | 6.02 | JUNB | MA0490.1 | chr15:67342669-67342680 | CTGAGTCACCC | - | 6.02 | JUND(var.2) | MA0492.1 | chr15:67341946-67341961 | TATTACCTCATCATT | - | 6.07 | STAT3 | MA0144.2 | chr15:67342750-67342761 | TTTCCCAGAAG | - | 6.62 | Stat4 | MA0518.1 | chr15:67342747-67342761 | CTGTTTCCCAGAAG | - | 6.01 | TEAD1 | MA0090.2 | chr15:67342029-67342039 | ATGGAATGTG | - | 6.02 | ZNF263 | MA0528.1 | chr15:67340429-67340450 | CCCTCCCTCTTCTCATCCCCA | - | 6.03 |
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| Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
SE_00035 | chr15:67339797-67344606 | Adipose_Nuclei | SE_02047 | chr15:67340168-67344425 | Aorta | SE_23212 | chr15:67340203-67343249 | Colon_Crypt_1 | SE_23998 | chr15:67340644-67342040 | Colon_Crypt_2 | SE_23998 | chr15:67342073-67342476 | Colon_Crypt_2 | SE_25827 | chr15:67339819-67342880 | Duodenum_Smooth_Muscle | SE_26536 | chr15:67340170-67344435 | Esophagus | SE_27694 | chr15:67339360-67344398 | Fetal_Intestine | SE_28551 | chr15:67339108-67344509 | Fetal_Intestine_Large | SE_31411 | chr15:67340035-67344784 | Gastric | SE_34728 | chr15:67339538-67344339 | HeLa | SE_36559 | chr15:67340255-67343228 | HMEC | SE_36917 | chr15:67339995-67343855 | HSMMtube | SE_42172 | chr15:67340158-67344220 | Lung | SE_45534 | chr15:67339352-67344348 | Osteoblasts | SE_47100 | chr15:67329410-67344315 | Panc1 | SE_47731 | chr15:67340625-67342538 | Pancreas | SE_47731 | chr15:67342555-67343029 | Pancreas | SE_48704 | chr15:67340401-67343412 | Right_Atrium | SE_50064 | chr15:67340158-67343295 | Sigmoid_Colon | SE_52244 | chr15:67340357-67343350 | Skeletal_Muscle_Myoblast | SE_52344 | chr15:67339569-67344423 | Small_Intestine | SE_64018 | chr15:67340343-67343392 | HSMM |
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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 |
GH15I067047 | chr15 | 67339355 | 67344348 |
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Enhancer Sequence | ACAATGAGCC ATGATTGTGC CACTGTACTC AGCCTGGGTG ACTGGGTGAC AATGCAGGAC 60 CTTGTTTCAA AATTTAAAAA GGATGAGCCC TTCAGCCTTC AGCCTAAAAG TCTGCTCACC 120 ACTATCACTC TACATTGTGA ATTAACCCTT CACGTGCAGC CCTCCCTCTT CTCATCCCCA 180 GCTAGACGGC TTATTGGTGT ATCCTCAACT GTCCAGCTAA TAGGCTTGTT GATACGTTGA 240 TTCACTGATG AATGACCCTT TGAATAACTT GGCAGCATCA TCTCATATTT GTACATTGTA 300 CAGTTCACAA AACAGGTTCA TAGCTATCCT TTGCTTCAAA ACTGCCAACA CAGAGCCTCA 360 AGGATTATGT GGTGGAAGAA TCACTATCCT CACTTCACAG AGGTGATCCT AGGTCTCGGG 420 GAGATGAGGA GGCTTGAGGT CTTGTGACTG GGTGCTGGCA GATTGGAACT TGGACCCAGG 480 CCTTTGAATC CCGGCATTGT GCCAACTCCA CTGTTGAGTG TGGCCTGAAA ACACGGCCTT 540 AATCCAGCCG TTAATTAATA ACTAACTTGT GTGTTGGCCT CTGCAGTTTA CAAAGTCTCT 600 CCCTTAGGTC ATTTCTTTTA ATCTCCACAA TCCTTTGGTG GCTGGATGTT GTTATTATTT 660 TCCCCCAACC TGTCCCTTTG CAAAGAGGGG AAACTAGTGC TCAGAGGGTT GAAGTGTCTT 720 ACCCAAGGGC ACACAACTAT GGCTACAGAG CTACACTCAA TACCCAGCTT CCAGCTTCCC 780 TGTCCTCTGT TCCCCATCCT CTGTTCCATC CCTCACTTTT CTTCCCATGG GCAGGCCCTG 840 GAGATGTCTG AGCATGTGGG CTTTTCAGCC ACCCTCCAGC AGCCTGAAGG CCTGGCTCTC 900 CTGGGCAGGC CCAGGAAACG CCTGGCTCAG TGGTGCTGAG CAGCCCCTCC CATGAGGCCT 960 CGAGTTGTTT TTCTTATCTA AATAAACTCT ACACAAACAT GGGCACATTA CTCATGTGTG 1020 AGTTATTTGC GATAGCATAG CCCAGAGATG GGGAAATCAG TTCACACTGG AACTATGTCT 1080 CAACCTGGTC AAAAAACAAA TGGGGAAATG GAGTTCTAGG CCCAGGGCAG CAAAACTCAA 1140 ACCCACACCC CATCTCAAGC CCAGGGAAAA CTTCTGCCCC TGGTCACATG CTCTGTGGAC 1200 CCCACTGGAG GGAAGACAGA ACCCACCTGT GCCTAGGGAA GGACATGAGG GAGCTCCAAG 1260 GGGTGGGCTC TCGCTTCCAA GGCCAGCCTC TCTTCCCACA GGCCATCTTG AGGAAAGACA 1320 GAGACACACC CGCAGAGCAG GAGATCTCTG CTTTATCCTC TAAGCATTTT GCAAAATGAG 1380 TGCTGGAATC CATACCTGGT CCTTCTCCCC ACATGTAATT AGATTCCTTC AACTTTTGGA 1440 CTTGGATCTT TCACCAGAAG GCCTTGAGAT CAGGGGAGGG GCTTAAGGAG CTGCTATATA 1500 AATGAAGACG TGTAACTTAG CTCAGTGCCT GGCAGGGACC GGCTGCTTTC ATTACGGTTG 1560 AGGGGCAGTT GTTTGTGTGT GTGATGGGAA AGAGAGATGA TGCTAAAAGC TGTTTATCTT 1620 GGCCCACCAT CACATACCTT CCCAAAGGCT TACACACCCA CTCTCTCAGG CATGTTTATT 1680 ACCTCATCAT TTAGGTGAGG GCCTCTCAGA GAAGTTCTAT GATGTGCTGG AGGTACCCAC 1740 GGGATGTCAG TCATAAACCA TGGAATGTGG GTTTTGTGTT TGCAAAGGGC TCTTGGACAC 1800 AGGATCTCAA AGGAATTCTT GACAGAGCTA GAAAAAGAGC CTTAGCCCCC TGACCCCTAG 1860 ATCAGCAGAT TTTGCTTCCA GAAAATGTTT CTAGGATGCC CAGCTCTCTG GATATGACTC 1920 ATATTGGTCC CAAGGAATGA CAGCCCTGCA CATGGCTTCT GCCCCAGGGC TCTGGAACTG 1980 TGCTGCCTGG CCCCTGTGGT CACAGGGATT CCTTGCTCCT CTTTACCAGC TTCAGACCAA 2040 GGGACTCGAG CTTGGAGAGG CTGTGGTTAC TGTGCTGCGT GGGTCTTGTC CTGGAGACCT 2100 TGTGTGATTC ATCTTCGTGT TCCCACAGGG ACTGTCACTA AGACAGGGCT GGGTTAAGAC 2160 CCTTAGATAT CCTGAAAGAT CAGTCCTCCC TCATATGAAA TTCAAAGAAA AACAATTCTA 2220 AATCTGAAAA AAATGCCACC CATCCATGTG GGCTGAGCTC AAAATAGCTT CCTTCTAGAG 2280 ATTTTGATTG CAAAATCCTG GATGAATGCA ATAAAGCTGA ACTTTTTTCC TTGGCCTAGG 2340 AGTGGGGCAA GGAAGGGAGG GGTTTTGCCA TTGGTCTAAG CACCTACTTG CTCTGCTTCC 2400 TGAGTCACCC AGATTGCCAA GGGGGTCTTG TACGTGGTAG ATGTCAGCCC ACGTCTTCTA 2460 AATTGAATGA CGTGTGCCTG TTTCCCAGAA GAGGAATAAA TCCAAGCAAT AATGTGTCAA 2520 AGTATGGGCA CAGAGTCTGA GCCAGCAAAC ACACACACAC ACACCCATGT GCACCCGTGC 2580 ACACACAAAC ACAAGCCCAT GCAGGTACAC AGAGGGGAAG 2620
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