Tag | Content |
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EnhancerAtlas ID | HS055-02672 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr14:94431210-94433900 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxq1 | MA0040.1 | chr14:94431519-94431530 | CATTGTTTATT | + | 6.02 | HNF4G | MA0484.1 | chr14:94432469-94432484 | GGAGGTCAAAGTTCA | + | 6.98 | Hnf4a | MA0114.3 | chr14:94432470-94432486 | GAGGTCAAAGTTCACT | + | 7.5 | NR2C2 | MA0504.1 | chr14:94432469-94432484 | GGAGGTCAAAGTTCA | + | 6.72 | Nr2f6 | MA0677.1 | chr14:94432470-94432484 | GAGGTCAAAGTTCA | + | 6.83 | Rxra | MA0512.2 | chr14:94432470-94432484 | GAGGTCAAAGTTCA | + | 7.38 | STAT3 | MA0144.2 | chr14:94432352-94432363 | CTTCTGGGAAG | + | 6.14 | STAT3 | MA0144.2 | chr14:94432375-94432386 | CTTCTGGGAAG | + | 6.14 | YY1 | MA0095.2 | chr14:94432851-94432863 | GCAGCCATCTTG | - | 6.74 | Zfx | MA0146.2 | chr14:94433556-94433570 | CTGGCCCAGGCCTG | + | 6.14 |
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| Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
SE_01812 | chr14:94430073-94431963 | Aorta | SE_01812 | chr14:94431977-94438020 | Aorta | SE_16780 | chr14:94424755-94431660 | CD4_Naive_Primary_8pool | SE_26176 | chr14:94428569-94433222 | Duodenum_Smooth_Muscle | SE_26176 | chr14:94433522-94438312 | Duodenum_Smooth_Muscle | SE_27221 | chr14:94431897-94434108 | Esophagus | SE_40684 | chr14:94428614-94438317 | Left_Ventricle | SE_42615 | chr14:94431841-94438199 | Lung | SE_48057 | chr14:94427314-94438298 | Psoas_Muscle | SE_48827 | chr14:94431890-94432882 | Right_Atrium | SE_49510 | chr14:94432094-94432559 | Right_Ventricle | SE_50919 | chr14:94433228-94434711 | Sigmoid_Colon | SE_51124 | chr14:94421388-94433866 | Skeletal_Muscle | SE_52728 | chr14:94428584-94435421 | Small_Intestine | SE_54605 | chr14:94431051-94433895 | Stomach_Smooth_Muscle | SE_58336 | chr14:94405869-94468889 | Ly1 | SE_58879 | chr14:94405876-94468971 | Ly3 | SE_59615 | chr14:94417819-94449507 | Ly4 | SE_60397 | chr14:94402665-94450746 | DHL6 | SE_62757 | chr14:94419629-94446114 | Tonsil |
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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: 2 | ID | Chromosome | Start | End |
GH14I093966 | chr14 | 94432939 | 94436091 | GH14I093953 | chr14 | 94419761 | 94432931 |
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Enhancer Sequence | AGCTATATAT TATCTACCTT CCCATCCATC CACCCCTCTA TACATATATT CAACTATCCA 60 ACTACCCACT CAACCACCCT CCATCTATCC TCCTATCCAT CCATCTGTCT ACTCATCTGA 120 CCATTTATCT GTCTATTCTC TCAGCACTAC TCATCATTCA TCCATCCATT CATCTTTCTA 180 TCCGTCCAAC CATCCATCCA ACTGTCCTCC CATCCCTCCA TTATCCTATC TGTCCACCCA 240 GCCATCCATT TATTCATGCA TCATCACATC CACCCACCAT ACATCCATCT ATCCAATCAT 300 CCACTCATCC ATTGTTTATT TTTCCATTCC AGATAACCTA TCTATCCATG TATTTATGCT 360 CACTTGTTGA GCACCCACTC TGTGTCAGGC ACTCTTCTAA GCACTGAGGA TACAACGATG 420 ATTCCAACAG ACAAAAATCC TTGCCCTCAT GGAGCTTACA CAGGATTGCA TACCAGTTAC 480 CAAGAGCATA GATCCTGGCA TTTCTCCATT TCTTTGCACT GTGATGGGCC TGAGAATACC 540 AGAGATGAAT CAGACACAGA CCCATTACTT CAAATCACAT GATCTAGTTA AAATCAGTCA 600 TTAAAATAAC GTCCCATGTT AATTCCAGTG ACTCTTTTCT TAAAAATGCC TCAAAGAGTA 660 ATAGACTCCA GTTGGGTGCC AATGCTTTAA GAATATGAAG TGGAATCAAC TAAGCTTGAT 720 TTTCATTCTG GCTGGCTGAC TCACACTGTG TGGGTCAATG GTTCTTGGTC CTGGCTGAAC 780 ATTGAATCAC ATGGCCCTCT AAAAAATACC CCGAATACCA GTGCATTACT TTGATTTGTT 840 CAGCAAATAT TCACTCCCTT TCCCTAAAGG CAGATCTTTC CCCACCCTTC CCTGTTGATA 900 TGGGTCTCAA TATGCATGAC TTGCCCTGGC CTGTGAGGGC TGATGGACAT GCGTCAAGGA 960 TACACATGAC AAGTATGTAC ACTGGGGTTT GCTCTTGCTC CTCTGCCATC ACCAAGAGAA 1020 GAGCTTCCCA CTGGAGCTTG CTGCCCCTCA GCCTAGGCCC CAGAGAGAAC ACACCCGGGC 1080 ACCTGAGCCC AACCTCCTCA GAGGAGCCTT CTCCTTCTTC AAGGCCCAGG GCAAGTGCCC 1140 CTCTTCTGGG AAGCCGACCC AGATCCTTCT GGGAAGAGGA ACTTCTCCTG AGCTGTGGTC 1200 AGTAGTTCAT GGGTGGACTT GACCCTGGAT CCTCTTTCCA AGGCCAGCAC CTTATGTGAG 1260 GAGGTCAAAG TTCACTGCAT GGCTGGCCAA ACAGCTCCAT TTTCATAGGG TGTGGCAGAT 1320 CCTGCGGATA GTCCCCTCAA TGGCCATTTC CCCCATCTTC CCTGATAGCA GAACCTGGCT 1380 TTGTCTAGGC AACAGGGTGC CCTGTCCCAT GGATGAGTCA TGACTGCTTC AAGCCAGGTG 1440 GGACAATCTC ACCGCCTCAG CTGGTGACAA GTCCAGGGGT GGGACTGTAG CCTAGTTTTA 1500 TCCAAAGAGT TATAACAGAA AATCTGCTGG GGTGCTCCTA TGGAAGACTT TCCTTTCTAA 1560 TAAAAGAGAG AGTAGTGAAC AAAATGATTC CTTTCCCCAA CCTCTGCTTA GTGCTTGGAG 1620 GACTTGATGC TTGGAGTGGC AGCAGCCATC TTGTGACCAT GAGGGGGACA GTGAATGACA 1680 GGTTGATACA ATGAGTTTGG CATAATGAAT AATAGTTTTT CTGGGTCCTT CATTATGTTG 1740 CAGAACTGCT GAACCAATGC TGGGTCCGCC CACCCTAGCC TACTTGTTAG GTACTGAAGA 1800 TTCTTGTGGT TTAGCCAATG TTAGTTGGGT TTTCTCTTAT AGGCAGTCAA ATCATCTTAA 1860 CGAATGTCTC TCAGGCCTGG CTGAGAGTCT TGAAAACATG TCAAGGACCT GGTTCAGCCC 1920 TGAATCAATG AACTCAAAGC CTCAGGGCTG GGACCCAGGG AATGCAATGC TAGAGGCTTC 1980 TCTGGTGATG TTAGTGTGTG GCCAGAGTTG AGAACCCCTG CTCAATGAGA TTAATATGTC 2040 AGGTGGCCAG TCTGTGGTCC ACACTAGAGG AGGGGAAGGG TCATGACCTC ACAATCATTT 2100 TATGCCCGAT GCTTGGAGTG CTGTTATTTA CAGCAGTAGC AGCAGTTTTA TTTATTGTGA 2160 AAGGAGCCCA GGACAGGGAA CCAAGGGACT TGGGTTTCTG TCCCAAGTCA GCCATGAGCG 2220 CCTCTCTTCC TCTCTTGTGT CCTCAGTTTT TCCATCTGTT AAATGGCAGG GTAGACTAGA 2280 GCCTGTCCTC TGGCCCTTGT ACTGGCAGGA GGTACCTGTG CAGCTGGGTG GAGCCCCCAT 2340 CTCCAGCTGG CCCAGGCCTG GCTTCCCACT CCTTTGTTGC TTCTCTGAGG CTGGGGTCCC 2400 TGCCAGGTCT GAGTTGGCCC AGGTCTGCCT TCAGTGGCGG GGGGAAGGGG CTCTGCCCAG 2460 TGAGGTATGA CACCCTTCTC TTCTCTAAAG CTGGTCTGGC TTTACATACC CCACCGCCTG 2520 GTGCAAGGTA GGGGCTCAGT GCACATGGTG CTGAACTAGC AGGAAGTGCT GGTGCCCAGG 2580 ACCTGGCCTG GCATCCTGGT GCCACCATCT AAAGGTGTCT GCTCAAAGCC AGGGCACAAG 2640 GGGGAAGAGC ACTGCACTAA GAGTCATAGG CTGAGCTATA ATTGCCCTGC 2690
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