Tag | Content |
---|
EnhancerAtlas ID | HS044-10176 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr5:1101660-1104560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr5:1103465-1103483 | GGAAGCAAGGAAGCCTGG | + | 6.06 | GLI2 | MA0734.2 | chr5:1102691-1102706 | CAGCGTGGGTGGTCC | - | 7.1 | RREB1 | MA0073.1 | chr5:1101894-1101914 | CCCCCCTCCACCCCCCGACA | + | 6.16 | RREB1 | MA0073.1 | chr5:1102988-1103008 | CCCCCACCCAACCCCACTGC | + | 7.16 | ZNF263 | MA0528.1 | chr5:1102526-1102547 | CATCCCTCCCCCTCTTCCTCC | - | 7.23 |
|
| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_23448 | chr5:1101902-1102719 | Colon_Crypt_1 | SE_23448 | chr5:1103184-1105197 | Colon_Crypt_1 | SE_23989 | chr5:1102125-1103137 | Colon_Crypt_2 | SE_23989 | chr5:1103392-1105150 | Colon_Crypt_2 | SE_24840 | chr5:1102018-1103478 | Colon_Crypt_3 | SE_24840 | chr5:1103642-1105300 | Colon_Crypt_3 | SE_28283 | chr5:1102066-1103155 | Fetal_Intestine | SE_28283 | chr5:1103691-1112207 | Fetal_Intestine | SE_29290 | chr5:1101813-1103421 | Fetal_Intestine_Large | SE_29290 | chr5:1103664-1109497 | Fetal_Intestine_Large | SE_31577 | chr5:1101801-1105240 | Gastric | SE_40750 | chr5:1098688-1112458 | Left_Ventricle | SE_41639 | chr5:1103271-1105102 | LNCaP | SE_42534 | chr5:1098973-1112501 | Lung | SE_47233 | chr5:1089215-1112103 | Panc1 | SE_47514 | chr5:1103424-1103792 | Pancreas | SE_47514 | chr5:1103979-1105101 | Pancreas | SE_48976 | chr5:1101390-1112419 | Right_Atrium | SE_49487 | chr5:1101906-1103325 | Right_Ventricle | SE_49487 | chr5:1103361-1105151 | Right_Ventricle | SE_50482 | chr5:1101838-1112417 | Sigmoid_Colon | SE_52622 | chr5:1101898-1105202 | Small_Intestine | SE_53895 | chr5:1098905-1112484 | Spleen | SE_57916 | chr5:1102152-1103075 | VACO_9m | SE_57916 | chr5:1103217-1104833 | VACO_9m | SE_61441 | chr5:1092795-1176993 | Toledo | SE_65274 | chr5:1098822-1105236 | Pancreatic_islets | SE_69167 | chr5:1097016-1105179 | H9 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 1102623 | 1102762 | chr5 | 1101948 | 1104216 |
|
Enhancer Sequence | CCTCAGCCAT GAAGGCGGCG AGGTCAAGCC CTGGCCTGAA GAACTGGCCA CAAGTCAGTT 60 TTTTCTCGTC TTATTTTTTC TACCTCTTCA TTTTATTATA AAAACGACCC CAGGTAAGCA 120 AGTGGGCAGA CACCCTGTGC AGCCCTATGG GTGCTAGCTG TCCACGCACA GATCCGCCCC 180 ACACAGCCCT GGTCTGATGC ATGTCATGGC ACACAGTGGC CACCACTGCC CCGACCCCCC 240 TCCACCCCCC GACACTAAGC AGCCTTGTGG CCCTCCGGAG CCGCTTTGCT GAGTTTTCTC 300 TGGCTGCAGC CGCCTGGGCA AGAGAACGTC TATCTGCTGA GCATTAACAA AGGCCTGCCC 360 CTGCTCACCG GACCTACCAA GAGCCTCCCA CCACTTCCCC AGCTCCCTCC CTGCCAAGCC 420 CCCCAGCCAC AGAGGCAACC TCCGGTCTGT TTTTCACTCT AGGTTAGTTT TCCAGACACC 480 TTATCAACAA AGTGAATGCA GACCCTGTGG TCAGTAAGCA GATCCTGATG GGCTGGGCCC 540 TTGGGGAACA GCCTCCTGGG CTTGTCCAAC CAGGCTGTGT CCCCACCCCG AGAGGGAAGG 600 AGGCGGCTGC AGGTGGAAGG GCAAAGACCA GACACACGAG TGTCCCGGCC AGAGGAGGGG 660 CAGCCCCTCC AGCCAGAGAG GCAGTGAGAG TGTGTGTGTC AGATCCCTGA CCCATCCCGA 720 TCCAGGCCTG GGAAGTGCGT TCATGGGTAG TTTCTGCAGG GAGAAGCTGG CTCACCTCCC 780 TAATCGGCCC TAATCCCCTC TGAGATCACA ATGCCTCCAT CAGCCTCCCT ATCTCCAGGC 840 ACAACCTCCT CCCTTTCTCA GTGGCTCATC CCTCCCCCTC TTCCTCCCGC GTTTTGGGAT 900 TTTACAGCCA TTCTCCGCAA AGGGCTCTAG GAACGTCCTC TTAGACTCAG CCTCAGCCGG 960 AAGCAGCTGA CAGGCAGGAG GGGCTGTGAA GCTGAAGCCA GGTCCGACAG CCTCCGCCCC 1020 TTCCTGCCCT CCAGCGTGGG TGGTCCGTCC AGCTACCCAG CCCTGCAGAG CAGTGGCGGG 1080 TGGCACCGGA CCTGTGCACA CAGAGAGGCG CCGGGCCTGG GGCAGGGGAC AAGCAAGTCC 1140 AGGCTTCCCG GCTCCCTGCA CTCGAGGAGG TTCTCAGGCC TGGCTCTGTG TGTCCCCTGG 1200 GTCCAGCAGG CCACCCTCCC CTGGAGCCAC AGGGGACTCA CAGCAGAATG AGTCCCACCT 1260 GGTGACCCAG TGGCATCAGC TCACGTGGCC TCTGGGGACA GCCCGAGACT GAATGGACCC 1320 AGGAGCACCC CCCACCCAAC CCCACTGCCT GGAGGCTGAG TTCCCTGTGA AGGCGCGAGG 1380 ACCCAGGAAC ACTCCCAACC CCACTGCCTG GAGGCTGGGC TCCCTGTGAA GGTGCCGGGC 1440 ACTGAAATAA AGTGTGTTTA GGTTCCAGGA TCCGAACGCC AGCTGACGAC CCCTGGCCCT 1500 TGCCCTCCCT CTGCCCCTCA CAGTTTGTGC TGTGTGGGCC CCTAAAATCT AGAAACTGAG 1560 GCTCTCAAGG GGCACAGGAT GAGAACGGCC CAGTGTTCAG GCTGGGACAC GGGGGGCTTC 1620 AGGCAAGCTC TCAGGCTTCC AGCACAAGTT TCTGGCTAAA GCAGCGCTGC CTTCTGAGGG 1680 AAAAACAGGC CCTTCATCAC CCATTCCCGA AGTGACCTCA TCCCAACAGT CTGTGCAGAC 1740 ACCACCGCCA GTATCCTGTA AACCAGGAGA GCGCCGGGAG ATCCCAGCTC ACCGTCAGAG 1800 GCACTGGAAG CAAGGAAGCC TGGCTGGAAG GTCCTGGCAA GCTATGGCCA GACACACATG 1860 AACACACGCC ACAGAAAATA TACACTCACA TGCACAGAGA CATGCATGTG TACACATGCA 1920 CAGACAGGCA CTTCCACGTG CACACGCAAA CTTGCTCACA CGGAAGACAC TCTCCATACC 1980 CATACTCACA CGCTTCCCCC CTCATTCATA CACACAACAC TCACCTCGCA AACCTGCACA 2040 CGCACCTGTC CTCACATGTG CATACCCATA CCCGCAGTCA CATACACACA CCAACACCCG 2100 CACATACACG TGTACACACA CACATACCTG CAGCACACAC ATCTGCACAA AGTCCCAGGG 2160 GCTACAGCCC CCAGACTGCA CGACCCACGG GGCGGGGTGC CCAGGACACA GGCATGCACT 2220 GGGACTACAG CCCTTCCATC TAAAGGACAC GCCTGCTCGC GGGAAGGTGG CCTCGGGTGA 2280 ACTCACTTCC CGAACCCTCT GTCACGTGGC TGTTTGCTGG TCCTGGTCCA GCCTCCTCCC 2340 TCAGCAGCCA GAGTGACGTC TGAGCCATGG AGGGGCCGTG GGGTCCCCTA GTTCCAGAGA 2400 CTCGGGGCCC AGGCAGCCTG CAGGAGCAGA GATGAAGGAA GGCGGGAGAG GCAGGGCCCC 2460 CAGCGCACCT GCCAGGCCCT CCCAGGGCGG CTCCTGTTAC AGGCTGCCTC TGGGCTGCGG 2520 TCGGGGACCC TTGGCGGCAT GGAGGGGACC CAGGAGGGGC CTGGCCTGGC GCACTTCCCT 2580 CCTCCGATTT CCACTCCACT CAATCCCTCC CCAGTGACTG CCCAGGGCGT CTCTGAGCCT 2640 CCCTGAAAGC CCAGGCCCGA CCCGCTGGCG CCAGAGGTCT GCAGACAGAG CCAAGGAGAT 2700 GAGAGGTCAC AGCCACCGCC ACCCTCGTGA CAGGCTGGCT CCTGCCAAGG GAAACTGAGG 2760 CACAGAGCAA ATGTTCAAGG ATCACTTTAA CAACCTCCTC CCGGCTGCAC GTCTGCAAGG 2820 TGGACATCCC CTGTGCACGG GACTTAAATG GACAGGAACG CTGGGAGGGC CAGCGGGGCT 2880 ACCCCACCAT GAGGACAGCT 2900
|