Tag | Content |
---|
EnhancerAtlas ID | HS052-00014 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:997510-1000170 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:999343-999362 | GGCCGCCACCTGGTGGCCG | - | 8.19 | EWSR1-FLI1 | MA0149.1 | chr1:997559-997577 | CCCTCCCTCCCTCCCTCC | - | 6.03 | EWSR1-FLI1 | MA0149.1 | chr1:997563-997581 | CCCTCCCTCCCTCCCTCC | - | 6.03 | EWSR1-FLI1 | MA0149.1 | chr1:997531-997549 | TCTTCCTTCCCTCCCTCT | - | 6.16 | EWSR1-FLI1 | MA0149.1 | chr1:997519-997537 | CCTTCCCTCCCCTCTTCC | - | 6.17 | EWSR1-FLI1 | MA0149.1 | chr1:997555-997573 | CCTTCCCTCCCTCCCTCC | - | 6.94 | FOSL2 | MA0478.1 | chr1:999173-999184 | GGGTGACTCAG | + | 6.02 | Gata4 | MA0482.1 | chr1:998068-998079 | GGGAGATAAGA | - | 6.62 | JUNB | MA0490.1 | chr1:999173-999184 | GGGTGACTCAG | + | 6.02 | ZNF263 | MA0528.1 | chr1:997522-997543 | TCCCTCCCCTCTTCCTTCCCT | - | 6.06 | ZNF263 | MA0528.1 | chr1:997963-997984 | TGCACCACCCCCTCCTCCCCC | - | 6.13 | ZNF263 | MA0528.1 | chr1:997523-997544 | CCCTCCCCTCTTCCTTCCCTC | - | 6.27 | ZNF263 | MA0528.1 | chr1:997551-997572 | CACCCCTTCCCTCCCTCCCTC | - | 6.56 | ZNF263 | MA0528.1 | chr1:997527-997548 | CCCCTCTTCCTTCCCTCCCTC | - | 6.68 | ZNF263 | MA0528.1 | chr1:997516-997537 | TCCCCTTCCCTCCCCTCTTCC | - | 6.93 | ZNF263 | MA0528.1 | chr1:997555-997576 | CCTTCCCTCCCTCCCTCCCTC | - | 7.63 | ZNF263 | MA0528.1 | chr1:997519-997540 | CCTTCCCTCCCCTCTTCCTTC | - | 7.71 | ZNF263 | MA0528.1 | chr1:997559-997580 | CCCTCCCTCCCTCCCTCCCTC | - | 7.97 | ZNF263 | MA0528.1 | chr1:997563-997584 | CCCTCCCTCCCTCCCTCCCTC | - | 7.97 |
|
| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_24070 | chr1:999416-999769 | Colon_Crypt_2 | SE_24817 | chr1:997610-998481 | Colon_Crypt_3 | SE_24817 | chr1:999005-1000308 | Colon_Crypt_3 | SE_27529 | chr1:999243-999870 | Esophagus | SE_34539 | chr1:997968-1000257 | HCT-116 | SE_65935 | chr1:996609-1000366 | Pancreatic_islets |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I001061 | chr1 | 996971 | 1001049 |
|
Enhancer Sequence | CCCACATCCC CTTCCCTCCC CTCTTCCTTC CCTCCCTCTC ACACCCCTTC CCTCCCTCCC 60 TCCCTCCCTC CCTCAGTCAC TCACGGGTGT GGCTCTTTTT TGCTGACATT CTGGGCTCTG 120 GGGCTGCCGC CTGAGTACAA TGTAGTCCTG AGCTCCGGAG TCCAGTGCCA CAAAAGTAAG 180 GAGCAGTTGT GATCTCGGAC GTGGGCTCCG GGGCAGCCCT GACCTCATGG GGGGCTGCAG 240 ACTAGGAAGG TCCTGGGACG GGGGGGCTGT TCACCAGGAA GGGGCAGGGC TGCAGCCTCA 300 GCCTCCCCTC CAGATGCCGG CAGCACCAGC CTCTGCCTGC ATGGGGCCGC GAGGTTTGCA 360 GTGACATCCC CCGAGCTTCC TGACCTGCCC CGGACACGGA GCACGGCTCC CAGGGGCCGC 420 ACAGGCACCC GCTGGCCTCT CGGCCCCTCC CTGTGCACCA CCCCCTCCTC CCCCCGACCC 480 CCATCCCTCT ACTGAGTGTC TCAATTCCAG TGTTATGGAC CTGGGACGCC ACAGTGCGGG 540 GAACAGCTTC TGCCCTCTGG GAGATAAGAA CCCGTCGTCA GGCAGCTGGG CTGCTGAAAC 600 AGTGACCATA AGCTGGGCGG GCAGGCGCTC CTTCCCTCAG CTCTGGAGGC TGGAAGTCCG 660 AGATCCTGGC CGTGGAGGCT GGGAGGGGTG GAGTGGACGG GGCTGCTGAC AGCCTCGGGG 720 GCGTGTGGAG AAGGAGGGAG CCCCAGTGGC CCCAGGCCCT GCCACTTGGG GGAGAATTCC 780 AGCCCCTCTG TGTCCCTGGG ACCCCACAGC CCCTGGCCAG TGGCCATTCC CGGCTTCGAG 840 CACAGTGGCC TCAAGCCACC ATCGTGGGTG TTACCGTGGA AACAATGAGG GAGGTTTGTG 900 TGGGGCCAGA TTCCTCCTCT GGGCACTGAC CTGCTCTCCC CACTCCAGGT GGTTTCACCC 960 CAACATCAGC AGGGTGGAGG CGGAGAAGCT GTTCCTATCC AGAGGTCAGC GTGGGGACTT 1020 CCTTGCCAGG CCCAGTGAGA GCAGCCCGGG GGGCTTCACG CTGTCCGTCA GGTGGGTGGG 1080 CCCTGGCTGG GCATGGACAG GGTCTGGTTG AAGGCCTCCT GGAGGACCGG TGGGCAGCTT 1140 CCTGGACACG AGGACTTGGT GCGGGGGGCC GATGCCCTGG GAAGGTGGTG AGAGTTGGAC 1200 GTGGTGCTGG GCGGTCTCTG GGCAGGAAGG AACTATTTAG AGAGGCCCTT GGGGAGGGCT 1260 CATTGAGTCA GGGGCTCAGC AGGACCCTTT CCTCCCCTGT GAGGGCCCTG GGGACAGGCA 1320 GGGCCTCCGT GGCTGCGACC GTGTTGCCAG AGCCTGGGGG TGCAGCTGGG GAGTGCAGCG 1380 GGGTTCCCAT TGAGCTCTGG TACCCGCTGG GCTGCCAGGA CCCCGCGTTG GAGTGGTGAG 1440 CCCTGGCCCA GCATCCGCGT GTCAGCACAC GTGTGTACGT GTGCATGTGT GTGTTCGCGT 1500 GTCCATGTGT GTTCATGTGT GTGCGTGTGC ATGTGTGTGT GTGTGTGTGT GCGTGTGCCT 1560 GCATCCTGAG GGACGGCGTC TGCTAAGCAC TGGTTCAGGG CACAGGGTCC TGCACCTGCC 1620 TCCCTCAGGC CTCCTTCCTT CAGGTCTCAG GCACTGGAGT CCAGGGTGAC TCAGGGAAGC 1680 CGGTGCCTCC CCTGGCCCCA TCCCTGCCCT CCTGGCTGGT ACCCTGGGCT GAGCTGGTTC 1740 CTCCAGCCTC AGTTTCCCCA CTGCAGCGGG CTGCATCTGC AGAGAAGGAG ACCTGGTCTG 1800 GGGAGGCCCC TGGCCCCTCC TTGCTGAGGA CCAGGCCGCC ACCTGGTGGC CGCCCGCCCC 1860 TGCAGCGCCC GCCTGCCTCC TGCCGGCTCC TGGGTGGGGC GAGGGCCAGA AAGGCGAGCA 1920 GAGCAGCTCT GGGGCCCGGG TGGTGGTGCT GCCTGGACCC CCAAGGTCTG CGTATGTCTC 1980 GCTAAGCCTT CTGCCCTATC CGTGTGGGTC TCTCCCCCTC ACCTGGCCAG GCCGTGGCCT 2040 CCAGCCTCAC CTGTGCTCGC CTGTGCCTGG CCCAGGTGGT ACCACGGGCG CCTGTCTGGC 2100 AAGGAGGCTG AGAAGCTGCT GCTGCAGAAG GGGCATCCGG GCAGCTTCCT GGTGCACATG 2160 AGTCAGAGCG ATCCTGGGGG CTTCCCGCTG TCAGCGCTGA CGCAAGGGTG GGACGAGGCG 2220 CAGGGCTCAG GCCGCCAGCC ACAGGTCACG CACATCATGA CTCACTCCCA GGTGGGAGGG 2280 GGCGGCGAGC TGGGGCGGCC TCTGGGAAGG GCGGGCGGCC TTGGCCAGGC CCCTCACCGC 2340 CACCCCCACG GCCGGATGAG AAGTGGGAGA CGGGGAGCGT TTTGACACCC TCGGAGACCC 2400 GGTGTAGCAG GAAGAGCCCA TTGATGGGGA AGGTGGGGGC GGTTGTGCAC CTCAAGCAGG 2460 TAAAAGCCCC TCCACAGGCA CCAGGGCCGT GGGCACAGCC TCACCCAGGA AAGCAGCTGG 2520 GGGTCCACTG GGCTCAGGGA AGACCCCCTG CCAGGGAGAC CCCAGGCGCC TGAATGGCCA 2580 CGGGAAGGAA AACCTACCAG CCCCTCCGTG TGTCCTCCTG GCACATGGCG ACCTCCATGA 2640 CCCGACGAGG GTGCGGGGCC 2660
|