Tag | Content |
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EnhancerAtlas ID | HS129-11983 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr14:75720560-75722720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr14:75721314-75721332 | TCTTCCTTCCCTGCTGCC | - | 6.01 | Gata4 | MA0482.1 | chr14:75722505-75722516 | GGGAGATAAGA | - | 6.62 | IRF1 | MA0050.2 | chr14:75722069-75722090 | AAAAAAAAAGAAAAAGAAAAA | - | 6.09 | Myod1 | MA0499.1 | chr14:75721794-75721807 | AGTGACAGCTGCA | - | 6.78 | Myog | MA0500.1 | chr14:75721797-75721808 | GACAGCTGCAG | + | 6.62 | NKX2-5 | MA0063.2 | chr14:75720902-75720912 | CTCAAGTGGT | - | 6.02 | NR2C2 | MA0504.1 | chr14:75721097-75721112 | TGCCCTTTGACCTGA | - | 6.22 | Nr2f6 | MA0677.1 | chr14:75721097-75721111 | TGCCCTTTGACCTG | - | 6.2 | REST | MA0138.2 | chr14:75721820-75721841 | GGAGCTGTCCAGGGAGCTGTT | - | 6.63 | Rxra | MA0512.2 | chr14:75721097-75721111 | TGCCCTTTGACCTG | - | 6.03 | Tcf12 | MA0521.1 | chr14:75721797-75721808 | GACAGCTGCAG | + | 6.14 | ZNF263 | MA0528.1 | chr14:75721763-75721784 | GAGGGAGAAGAGGAAGGAGGA | + | 6.95 | ZNF263 | MA0528.1 | chr14:75721756-75721777 | TGGGGAGGAGGGAGAAGAGGA | + | 7.57 | ZNF263 | MA0528.1 | chr14:75721759-75721780 | GGAGGAGGGAGAAGAGGAAGG | + | 9.63 |
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| Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
SE_03033 | chr14:75721413-75722338 | Bladder | SE_23066 | chr14:75720639-75722614 | Colon_Crypt_1 | SE_23813 | chr14:75720702-75722314 | Colon_Crypt_2 | SE_25294 | chr14:75720698-75722657 | Colon_Crypt_3 | SE_25845 | chr14:75720731-75722804 | Duodenum_Smooth_Muscle | SE_26738 | chr14:75720693-75722454 | Esophagus | SE_27763 | chr14:75720628-75722691 | Fetal_Intestine | SE_28748 | chr14:75720612-75722548 | Fetal_Intestine_Large | SE_29571 | chr14:75720638-75722675 | Fetal_Muscle | SE_31671 | chr14:75720690-75722188 | Gastric | SE_35103 | chr14:75720377-75723240 | HeLa | SE_35974 | chr14:75718504-75727571 | HMEC | SE_43484 | chr14:75720676-75722668 | MCF-7 | SE_47575 | chr14:75720978-75722039 | Pancreas | SE_48476 | chr14:75720546-75722336 | Psoas_Muscle | SE_48750 | chr14:75720763-75722087 | Right_Atrium | SE_50151 | chr14:75720664-75722673 | Sigmoid_Colon | SE_51107 | chr14:75715241-75722998 | Skeletal_Muscle | SE_52363 | chr14:75720671-75722664 | Small_Intestine | SE_64641 | chr14:75720651-75727666 | NHEK |
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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 | GCTCACCGCA ACCTTCGACT CCCTGGTTCA AGTGATTCTC CTGCTTCAGC CTCCCGAGTA 60 GCTGGGATTA TAGGCATGTG CCACCACACC CAGCTAATTT TGTGTTTTTA GTAGAGATGG 120 GGTTTCTCCA TGTTGGTCAG GCTGTTTTCA AACTCCTGAC CTCTGGTGAT CCGCCCGCCT 180 TGGCCTCCCA AAGTGCTGGG ATTACAGGCA TGAGCTACTG CGCTTGGTCC AGAATTTTCT 240 TTTCTTTTCT TTTCTTTTTT TTAACAAACA AGGTATTGCT CTGTCTCCCA GTCTGGAGTG 300 TAGTAGCATG ATCATAACTC ACTGCAGTCT AGGCCTCCTT GGCTCAAGTG GTCCGCCTGC 360 CTCAGCCTCC CAAAGTGCTA GAATTATAGG TATGAGCCAC TGTGCCTGGA CAGATTTTGT 420 TTTAGAAGCA GGAGTTAAGT GTCCATGAGT AGTAGGAACT CAGGTAATCC AGCCCAAATG 480 GACTTGATCA ACCATCCCCT GATCCCGGAT CTCAGCGTGA TGGGAGTCTA GGAAACCTGC 540 CCTTTGACCT GAATCTGGAT GACGTTAGTA ATACAGGAAT AGGTGAAATG CCAGCCACAC 600 CTGGCTGGCC CATGAAAAGG AAATACTTCC CACGCTTTGC TTTTGCACAC CAAGGGCCCC 660 CAGGTAAAGG CATCCAGGGT GCAAGCCGCC TGCTTTAATG CCCGGGTGTG GCTGCAGGAA 720 CAACCCAGTA CAAACTGGAG TGAACCTGTT GCCCTCTTCC TTCCCTGCTG CCAAGCCAAA 780 CAGAACACAG GGAACACAAA TAGAATCATC ACAGTAAACC AGCTGTTGGA GCCAGACACT 840 GGGAGAACCC ACTCCCTGGC ACTGCCACCC CATTCACGGG TCCAGACATG ATGAAGTGCT 900 CTGAGGGCTG AGGAAGGTGT GGCCCGTGGG CATTCCTGTC CAGCAAGAAC CCCTCTGGCT 960 TGTCTGTATT CATTGCCACC CACATGGACC TCTCTATGGT TGCTTGCCAA AGCCGGGAGG 1020 GAGAAGGGTC TCCCCTTCCT CCAAGCCCAG GATCACCGGG AAATGCCCTT CCCACCTACT 1080 GGACTTGACT AATGCTGCTT GTCAAGAAGG GAACTCTTCA GACACATAAA AATCCTAAAG 1140 GTAGCTGAGG TTTGAAAGAA TTCGTGCTGG ACGTGCTTCC CTGCAGGGTC AGGCATTGGG 1200 GAGGAGGGAG AAGAGGAAGG AGGAGCTGGT TGTAAGTGAC AGCTGCAGAT AAATCTGTGT 1260 GGAGCTGTCC AGGGAGCTGT TGAACTCAGG TAGTGCCCTC CCTAGCCTGG GGCAGGTCAG 1320 AGTCTCCCCG AACCACCCAA ACCTTTCTGC TGCGTGTGCT CTGGGGCATG TCTCTCTTTG 1380 CCTCCTTGGA TCTTGAGCCA ATGAGGAAAT ATAGGCTAGT CCCAGAAGGC AGGGATGAAT 1440 TTGTGTTCTT TGTGGTGTCA GCACCTTTTC ATGAAGCTCT AGCAGATCTC ACAATCTTCC 1500 CTTCTTTAAA AAAAAAAAGA AAAAGAAAAA AGTTTGGAAA AGGGGGCTAG AGTCTCCCTA 1560 TGGAAAAGAA AGCTCGTGGA ATGATCCAAG TGGAGGTTTT CCATGCATTC CATGGCATCA 1620 TTGGAGATGT CCTGGCTCTG TACTTACTTA ACTACTTGAA TCTCAGTTTC TTCCGTTGTA 1680 AAAGTGGGCA CATGAAGACC TAGTTCTCAT GGATATTAAC AGGATAAAAC GAGATAACAC 1740 ATAGAGTACT CTCAAGTACT CTACATAGTC CTAGCATATC AAAAGTATTA GATAAATCTT 1800 GCCTTTATTT TCTCCTTCTC ATACACTGTG TCAGTGGCTT GCTGGGTCCT TGATTAGCCT 1860 GAAGGACTGA AAGAGAGACC TCAAGAGAGA GAATGGCAAA GTAAATACGA CCATCTTATT 1920 CGAACTTAAC TCTGCGTTTC AAGTAGGGAG ATAAGAAGGA CTGCTGTTCC ACTTCTTTTC 1980 TAGATGACAA GATGGGTTAT TTTTATTTTT TATTTTTGAG ACAGTTTCGC TCTTGTTGCC 2040 CAGGCTGGAG TGCAACGGCA TGATCTTGGC TCACCGCAAC CTCTGCCTCC CGGGTTCAAG 2100 TGATTCTCCT GCCTCAGCCT CCCTAGTAGC TGGGATTACA GGCATGCGCC ACCATGCTTG 2160
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