Tag | Content |
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EnhancerAtlas ID | HS002-07275 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr4:6934100-6935800 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr4:6934443-6934458 | GGGCTCAAAAGGTCA | + | 6.7 | Nr5a2 | MA0505.1 | chr4:6934426-6934441 | TGTGGCCTTGAACTC | - | 6.65 | PPARG | MA0066.1 | chr4:6935303-6935323 | ATTGAGCCACCATGACCCAC | - | 6.01 | ZNF263 | MA0528.1 | chr4:6934989-6935010 | CCTCCCTTCCCCTCCCCCTTC | - | 6.01 | ZNF263 | MA0528.1 | chr4:6934999-6935020 | CCTCCCCCTTCCCCTTCCCCT | - | 6.19 | ZNF263 | MA0528.1 | chr4:6935004-6935025 | CCCTTCCCCTTCCCCTTCCCC | - | 6.31 | ZNF263 | MA0528.1 | chr4:6935010-6935031 | CCCTTCCCCTTCCCCTTCCCC | - | 6.31 | ZNF263 | MA0528.1 | chr4:6935016-6935037 | CCCTTCCCCTTCCCCTTCCCC | - | 6.31 | ZNF263 | MA0528.1 | chr4:6935005-6935026 | CCTTCCCCTTCCCCTTCCCCT | - | 6.36 | ZNF263 | MA0528.1 | chr4:6935011-6935032 | CCTTCCCCTTCCCCTTCCCCT | - | 6.36 | ZNF263 | MA0528.1 | chr4:6935017-6935038 | CCTTCCCCTTCCCCTTCCCCT | - | 6.36 | ZNF263 | MA0528.1 | chr4:6934993-6935014 | CCTTCCCCTCCCCCTTCCCCT | - | 6.37 | ZNF263 | MA0528.1 | chr4:6934976-6934997 | TCCCCTCCCCTCCCCTCCCTT | - | 6.47 | ZNF263 | MA0528.1 | chr4:6934992-6935013 | CCCTTCCCCTCCCCCTTCCCC | - | 6.88 | ZNF263 | MA0528.1 | chr4:6934966-6934987 | TCCCCTCCCCTCCCCTCCCCT | - | 6.91 | ZNF263 | MA0528.1 | chr4:6934971-6934992 | TCCCCTCCCCTCCCCTCCCCT | - | 6.91 | ZNF263 | MA0528.1 | chr4:6934998-6935019 | CCCTCCCCCTTCCCCTTCCCC | - | 6.98 | ZNF263 | MA0528.1 | chr4:6934980-6935001 | CTCCCCTCCCCTCCCTTCCCC | - | 7.03 | ZNF263 | MA0528.1 | chr4:6934986-6935007 | TCCCCTCCCTTCCCCTCCCCC | - | 7.8 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27664 | chr4:6935512-6939740 | Fetal_Intestine | SE_28549 | chr4:6927396-6934981 | Fetal_Intestine_Large | SE_28549 | chr4:6935127-6939692 | Fetal_Intestine_Large |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 6934311 | 6934976 | chr4 | 6935047 | 6935201 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I006932 | chr4 | 6934108 | 6951477 |
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Enhancer Sequence | ATTAAAAAAA AAAAAAAAGA CTTGAAGATG TCAGTGACAA AGTTAACCAA GCAGGTACTT 60 GGAAGGAGAG TGATCCAGCA AGGGAGAAGG ATGCAGGCAG GCCTGATGCA TTTGAGCACA 120 GATGCCCTGG GGATGGACAG AGAGAAGGAA GGGATAGGGT CAGTGGGACC AGATTCTGTA 180 TGGGCATGTA GGCCACTGTG TGATGTTGGC TTTGACTTAG ACTCAGTGGG GAGCCACTGC 240 AGAATTTTTG TCTTTTCGAG ATGGGGTCTT GCTGCATTGG CCAGCCAGGA GTCCAGTGGC 300 CATTCACAGG TGCAGCCATA GCGCAGTGTG GCCTTGAACT CCTGGGCTCA AAAGGTCATC 360 CTGCCTCAGC CTCAGAATAG CTGGGCCTAC CACACCACTG TGCCTGGCTC TACTGCAGAA 420 TTTTGAGCAG AGGAGTTGCC GTGGTGTTTT GCTGCTGCAT AACAAATAAC CACACATTTG 480 GTGGCTTGAA ACAACATGGC TGTCCATCAT GGTGTGGCTG GGTTCCCCTC GGGCACTTAT 540 CAGGATGAAA CAGCATGTTG GCGGCTGTGT CCCCGTCCCA GTCTTGGCTA AGGAATTGTC 600 TGCTTCCAGG CTCACTGAGG CTGTTGGCAG AGCTCGTTGT GGCTATAAAC TGAGCTCATC 660 ATTTCCCTGA TTGCTGTCAG CTGAGGGTCA CTTGCAGCTC CTAGAAGTCA TCCAAATTCT 720 TTGCTGTGTG GCCCCTCCAT ATTGAAAACC AGCAACAAGG CTTCTTTTGT GTGGAGTCCA 780 TCTCACACTC CAAATCTCTT CCCAGAGAGA ACACTGATTG CTTTTAAGGG CTCACTGAAA 840 TTGTGTAAGG CTCATTGAGA ATTACCTCCC CTCCCCTCCC CTCCCCTCCC CTCCCTTCCC 900 CTCCCCCTTC CCCTTCCCCT TCCCCTTCCC CTTCCCCTTC CCTTTTCTAG AGGCAGAGTC 960 TCGCTTTGTC GCCCAGGCTG GATTTCACTG GTGCCATCAT AGCTCACTGC AGACTTGAAC 1020 TCCCAGGCTC AAGCCATCCT TGCACCTCAG CCTCTGGAAC AACTAGGATC ACAGACGTGC 1080 GCCATCACAC ACAGCTAACT TTTAAAATTT TTTGTAGAGA CATGGTCTCA CTTTGTTGCC 1140 CAGGCTGGTC TCGAACTCCT AGCCTCAAGT GATCCTCCTG CCTTGGCTTC CCCAAGTGTT 1200 GGGATTGAGC CACCATGACC CACTGTGCCT GGCCTACCTC TGTTTCTTAA AGTCATCTGT 1260 GCCATTTGAT GTAACCTGAT CACAAAGTCA CTGTCCCATC ATATTCATAG TTTATGCCTG 1320 TGTTCAAAGG GAAGGGTATG AACATCAGGG AAAGGGAATC TCAGAAGTCT GCCTGCCATA 1380 GGAGTAGTGA TTTCATTGAG TCCTAAACAG AATGCCCTGA GGTGCTGTAC TGAGAGGAGG 1440 CTTCCGGGCA GGGGAAGGGC AGAGCAGGGA GTCTGAGGAG GCTGTTGCAA GAGTCCAGAC 1500 AAGAGGTGAT GATGGCTTCA CCTGGGTGGC AGCTGTAGGG AGGGTGCGAT TTGAAGAATG 1560 GATGTGGGTG TGGAGAAAAG AAAGGAGTCA AAGATGACTC TGAGACTTTC GGCCTCAGCC 1620 AGTGGAAAAT AGAGTTGCCA AGTTGGAGTG AAGATGAGGG GTGGAGTTTG AGACATCTTA 1680 GACATTTGCA GGAAGGAGGT 1700
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