Tag | Content |
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EnhancerAtlas ID | HS052-00151 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:8257520-8258920 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata4 | MA0482.1 | chr1:8258010-8258021 | TCTTATCTCCC | + | 6.62 | HES2 | MA0616.2 | chr1:8257655-8257665 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr1:8257655-8257665 | GGCACGTGCC | - | 6.02 | NFE2L1 | MA0089.2 | chr1:8257947-8257962 | AGTGCTGAGTCATGC | - | 7.27 | Nfe2l2 | MA0150.2 | chr1:8257949-8257964 | TGCTGAGTCATGCAC | - | 6.66 | ZNF263 | MA0528.1 | chr1:8258739-8258760 | CCCTCTCCCCCACTTTCCTCC | - | 6.25 | ZNF263 | MA0528.1 | chr1:8258745-8258766 | CCCCCACTTTCCTCCTCCCCT | - | 6.39 | ZNF263 | MA0528.1 | chr1:8258766-8258787 | TCTCCTCCTTCTTCCTCTTCC | - | 6.59 | ZNF263 | MA0528.1 | chr1:8258763-8258784 | CCTTCTCCTCCTTCTTCCTCT | - | 6.63 | ZNF263 | MA0528.1 | chr1:8258753-8258774 | TTCCTCCTCCCCTTCTCCTCC | - | 7.12 | ZNF263 | MA0528.1 | chr1:8258759-8258780 | CTCCCCTTCTCCTCCTTCTTC | - | 7.27 | ZNF263 | MA0528.1 | chr1:8258756-8258777 | CTCCTCCCCTTCTCCTCCTTC | - | 7.5 | ZNF263 | MA0528.1 | chr1:8258769-8258790 | CCTCCTTCTTCCTCTTCCTCC | - | 7.77 | ZNF263 | MA0528.1 | chr1:8258742-8258763 | TCTCCCCCACTTTCCTCCTCC | - | 7.86 | ZNF263 | MA0528.1 | chr1:8258775-8258796 | TCTTCCTCTTCCTCCTCCTTC | - | 9.66 | ZNF263 | MA0528.1 | chr1:8258772-8258793 | CCTTCTTCCTCTTCCTCCTCC | - | 9.83 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_02150 | chr1:8257513-8259183 | Aorta | SE_33918 | chr1:8257041-8259053 | HCC1954 | SE_34231 | chr1:8248874-8265404 | HCT-116 | SE_34786 | chr1:8256055-8259168 | HeLa | SE_47106 | chr1:8252219-8265565 | Panc1 | SE_54787 | chr1:8257110-8266466 | Stomach_Smooth_Muscle | SE_55963 | chr1:8255991-8265376 | u87 | SE_65889 | chr1:8257508-8258772 | Pancreatic_islets | SE_67577 | chr1:8255991-8265376 | u87 |
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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 |
GH01I008196 | chr1 | 8256176 | 8259101 |
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Enhancer Sequence | GGTGTTGTGG CTCATGCTTG TAATTCCCAA TACTGAGGCA GGAGAATTGC TTGAGGCCAG 60 GAGTTCAAGA CCAGGCTGGG CAACATGGCG AGACCCCATC TCTACAAAAA TACAGAAAAA 120 TGAGCTGGGT GTGGTGGCAC GTGCCTGTGG TCCCATGACT CGGGAGGCTG AAGTGGGAGG 180 ATCACTTTAG CTGGGGAGGT GGAGGTTGCA GTGAGTTGAG CACTCCAGCC TGGGCTACAG 240 AGTGAAACGC TGTCAAAAAA AGAAAAAAGA AAAAAAAGAT ACTCTCTTAT ACATGCAGTA 300 TAATGATCAA AATCAGGAAA TCCAACATAA ACAGAATGCC CTTATCCAGC CCACAATCCA 360 CACTTGAATT TCATCACCCG TCCCTGCAGC TTTCCTGGCG GGCCTGGGCC CTGATCCAGG 420 ATGGCCGAGT GCTGAGTCAT GCACCCCTCT TCACCCGAAG CTCCTCCGCC CACACCTTGT 480 ACAGGCGCCT TCTTATCTCC CAGGTCCGAG TCTAACCGCA GCTCCCCACC TGCTCATCCT 540 TACGGGGGCG GAGATGCGGT CTCACAGTGC CTGGCTCTGT AACTTCAAAG CACGTGTCCA 600 CATCCTGGTC TGTCCTGTCC TCTCCACGAA AAGTGATCCC CAGGGTCAGG GTGTGCCTCG 660 TTGCCACTGC AGGGACTGGG CATCCAGACC CTGCAGGGGG GACACTGGGA TCACCATCGG 720 CCTCTCTGCT CATGAGCTGC GTGACCTTGG GCAACTTAGC CCTTTTGTGC AGCTGTAAAA 780 TGAGGATGGT GGCTGCACCC CATCTGGAGT TTTCTGAGAG GCAAACGGGT CTGTTATGAG 840 AATCCAATGA GTCCTTATGT GTAAAGCACT CAGGACAGTG CCGGGCACAT AGAAAGTGCT 900 CAGTAGGCCC GGCACGGTGG CTCACACCTG TAATCCCAGC ACTTTGGGAG GCTGAGGTGG 960 GTGGATAACT TGAGATCAGG AGTTCGAGAA TAGCCTGGCC AACATGTCAA AACCCTGTCT 1020 CTTCTAAAAA TATAAAAATT AGCCAGGCGT GGTGGCATGC ACCTGTAGTC CCAGCTACTT 1080 GGGAAGGTGA GGCAGGAGAA TTGCTTGAAC TCAGGGGGCG AGGTTGCAGT GAGCCTAGAT 1140 CACACCACTG CGCTCCAGCC TGGGTGACAA GAGTGAGACT CCATCTTTAA AAAAAACGAA 1200 AGTGCTTAGT AACCAAGAGC CCTCTCCCCC ACTTTCCTCC TCCCCTTCTC CTCCTTCTTC 1260 CTCTTCCTCC TCCTTCATAT TCATCCTCAC CATCTAGCAT AGTGCCTGGC ACACAGTAGA 1320 TACTCAAGGA AACCCCAGCA ATCTCTTCAG CAGTGGGAGG GCACAGAAAC AAGCGTGGGG 1380 AAGACGGGCA GAGCATTTAG 1400
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