Tag | Content |
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EnhancerAtlas ID | HS080-14905 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr17:46644520-46646970 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BHLHE40 | MA0464.2 | chr17:46646566-46646576 | ATCACGTGAC | + | 6.02 | RREB1 | MA0073.1 | chr17:46646861-46646881 | GGGGTGGGGGTGGGGTGGGC | - | 6.75 | TFEB | MA0692.1 | chr17:46646566-46646576 | ATCACGTGAC | + | 6.02 | USF2 | MA0526.2 | chr17:46646564-46646580 | GAATCACGTGACCGGG | - | 6.32 | ZNF263 | MA0528.1 | chr17:46646119-46646140 | GAGGGAGAAAGAGAGAGAGAG | + | 6.08 | ZNF263 | MA0528.1 | chr17:46646089-46646110 | GGAGGACAGAGGGAGAGAGGG | + | 6.15 | ZNF263 | MA0528.1 | chr17:46646107-46646128 | GGGAGAGGGAGGGAGGGAGAA | + | 6.17 | ZNF263 | MA0528.1 | chr17:46646111-46646132 | GAGGGAGGGAGGGAGAAAGAG | + | 6.24 | ZNF263 | MA0528.1 | chr17:46646105-46646126 | GAGGGAGAGGGAGGGAGGGAG | + | 6.26 | ZNF263 | MA0528.1 | chr17:46646115-46646136 | GAGGGAGGGAGAAAGAGAGAG | + | 6.49 | ZNF263 | MA0528.1 | chr17:46646786-46646807 | CCTCTCCTCTCTCCCTTCTCC | - | 6.55 | ZNF263 | MA0528.1 | chr17:46646406-46646427 | CTCTCCCTCTCTCTCTCCCCC | - | 6.77 | ZNF263 | MA0528.1 | chr17:46646789-46646810 | CTCCTCTCTCCCTTCTCCTCC | - | 7.34 | ZNF263 | MA0528.1 | chr17:46646795-46646816 | TCTCCCTTCTCCTCCTGCTTC | - | 7.91 |
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| Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
SE_00457 | chr17:46641810-46667072 | Adipose_Nuclei | SE_26192 | chr17:46641815-46655410 | Duodenum_Smooth_Muscle | SE_26972 | chr17:46643752-46661293 | Esophagus | SE_28820 | chr17:46639530-46679459 | Fetal_Intestine_Large | SE_38856 | chr17:46638491-46676520 | IMR90 | SE_44766 | chr17:46646373-46671210 | NHLF | SE_47101 | chr17:46628526-46699689 | Panc1 | SE_50647 | chr17:46631233-46657163 | Sigmoid_Colon | SE_54134 | chr17:46638493-46660923 | Spleen | SE_54898 | chr17:46643837-46661670 | Stomach_Smooth_Muscle | SE_63398 | chr17:46618362-46647118 | NCI-H69 | SE_68123 | chr17:46617997-46660074 | TC32 | SE_68124 | chr17:46617997-46660074 | TC32 | SE_68125 | chr17:46617997-46660074 | TC32 | SE_68126 | chr17:46617997-46660074 | TC32 | SE_68127 | chr17:46617997-46660074 | TC32 | SE_68128 | chr17:46617997-46660074 | TC32 |
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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 | TTCACCCACT ACCCACTGAG AATCCCTTGT TAACATGGAT GAGACTCAGT GTTCACTTGG 60 AGCAGAGTGT GGGAGCGAGC TCCTGGATGC TGCAGGGACT GGGGCCTAAG CTGCCACTCC 120 ACGTAGTGGA TGCCATGAAT AATTAACACC TGGGCGCGGC GTTGCTCTAA CTTCCCTGCT 180 CAAAGGTTTA CACTAGCAGG CAGAGTTAAA TATCACAGAT AATCGTGGCT ATAAAGTCAG 240 TTGGCCTGGC TCCAGTCAGG GAATGAGGGG CCAACAGCTG GGACTGGAGT TGGTGAAGGC 300 TCTGGCCCTC TGCACCTCAT CCATCACAAC TTTGGGGCAC AGTGCAGAAC ATTCCCCAAA 360 GCCACCTCTG GCTTTGCTCT TGACCAGCAG CCTCTCCCCT AGTAGGAAGG AACTGTGACC 420 TCCACATGAA ACTATAGGAG AAAGTTAACA GCTCTTCCCC TCCCTCTCCA ATCTGCACCC 480 CGTTTGCTCC CTTTTTGGAT GGGGACTTAG TTAAAAGAAC ACACCCAACA TCCTCCAACA 540 CTCCCAACTT TCTGGGACCA CCTGATTCCT AGAACATTTC TTTTCTAGAA AAACTTCGGA 600 GAACTTCTCC CCACTTTAGC CCCAAACACA GAGTCCCTCA CTGCTGAGGA AACTTTTCTT 660 TGTTTCAGCA GGTCAAAGGA AGGCTCCTGG GGTGTGAATT CATTTCCTTG TTTTGTTAGC 720 CAGGAGGGTG GGGAGCCAAA GCTTTCAGCT TCTCTCCCTG CCCTTCACCC TCTGCTTGCC 780 TCCATTGTCT CCCCCAATTT GGGTGATTCC TTTTCCACCT TTGACCACCC CCCAGACACA 840 TCAGTCCTAT AAATTAAGCT TTAATAATGT AACGGAACCC CTCCCATCCC TTTCCAATTG 900 CACAGAACTT TGATTTGGTC TCCATTGATC ACAAAAATAT TTGCCTTCAA CTCCAGTAAT 960 TTCTTTCTCC ACTTCCACCT CTCTTACTCT AAGGCTCCTT CTGCCTTCAG AGTTGGGTTT 1020 GTTCATCCAG GGCTGGAGTT GGAGAAGCCA AACTCCTGGA GGGGAGCTGC TAAAAAATGG 1080 AGCTCTGTCT GCTGCTGCAG GAATGTTGGC TCTATCAGGC TCACAAATAT AATTTTTATA 1140 TTAGACCATG GTCATTGACT GGGTTTATAT GCCAATGAGG CATTTCTGGT TTACCAAATT 1200 TATGAAAATC TCGCTTTAAT TGATAATCAC AGATGCTGTA ATTTAAGACC TCCAGCTATA 1260 GAGCTTTCAT ATTAACTGCT GATATATTAC TGTAAATCGT CTGAAATAAC CAACTCCTGG 1320 GAGCAGAGCA GAGAGGGAGG AAGTGCCTCC GAGAGCGACT CTCTCCCGGC CGGCCGCAGA 1380 AACAGCCCAG CTTCCACATC ATTTTCCGTG AAAAATGATT TATCGAAGAC ATGGCCATAA 1440 ACAACACAAC TCGCTCACAA ACACACGCAG ACGCGCACGC ACACACACGC GCGGACACAC 1500 ACACACACAA TGGCTGGCAT GCCGGCTGAG AAGCTGACAC CCATATTGCT ATAAATCAAG 1560 AAAAAGGTTG GAGGACAGAG GGAGAGAGGG AGAGGGAGGG AGGGAGAAAG AGAGAGAGAG 1620 AAAAGAAGAA TATTCCTAAA ATCTCTATGC AATGCCTCAA TGGGCATAAA CACACAGAGC 1680 ACCGTGTGAA GAGAAATGGC AGGAAATGAA GATGGCTATT TGTCACATTT TACGACAATA 1740 ACATTAATAA CAAACAATAA ATTTACATGG ACATATAAGA CGCGGTAGGT AGTGAGAAAT 1800 CCCTTCTACT TACAATACCC CAGCCCGCGG TGTGGCTCCG GCTGCGGGGC TGTTTTATTG 1860 CTGTCTCCCT TTCTTTCTCT CTCTCTCTCT CCCTCTCTCT CTCCCCCCTC TCTTTTTTTT 1920 TCTCGGGGTA CAGGCTTGTT TTTCAAAGGA CAGTTGAATT GCACGTCAGA AACAGGGAGA 1980 CCGAGCCTGC GATTTTCCTG ACGAATACAT ATCTATTCTG CAACCTCGGC ATTAATTATT 2040 TAATGAATCA CGTGACCGGG AGGGGGAAGG GGGTCTTTCG ATTTCAGGCT CAAAGGACCA 2100 CTATGACCTT CCCCTTCAGG AGGAGAAATT TTCCTGCAAA ATAAGTTCCC CCTCAACCCA 2160 CCAATGGAAC AGTAGTGAGG TCTCCGTCTG TCTCCCACAC TCACATCCAT ACCTACTACA 2220 TCTGCAGCTC CCTAACCCCC ATGGACACAC ACTTACCCAC AGCCCACCTC TCCTCTCTCC 2280 CTTCTCCTCC TGCTTCTGCT TAGTTCGTGG AGGTGCAGAA ATAGTCTGCA GGGGCGTCTA 2340 GGGGGTGGGG GTGGGGTGGG CTCAGAGCCC TTCTCCAAGC CCCTGGATTT CTCAGCTTCC 2400 AGTTCTTCTC TCTGCATCCT TTAGGATTAA GGTTCCCTCC CCAACTCCAT 2450
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