Tag | Content |
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EnhancerAtlas ID | HS167-03496 |
Organism | Homo sapiens |
Tissue/cell | Retina |
Coordinate | chr2:238570910-238573040 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr2:238571316-238571328 | GCTATTTATAGT | - | 6.11 | MEF2B | MA0660.1 | chr2:238571316-238571328 | GCTATTTATAGT | - | 6.74 | SP8 | MA0747.1 | chr2:238571480-238571492 | GACACGCCCACC | + | 6.02 | ZNF263 | MA0528.1 | chr2:238572669-238572690 | GGAGGAGCAGGGTGAAGGGTG | + | 6.06 | ZNF263 | MA0528.1 | chr2:238572666-238572687 | GAGGGAGGAGCAGGGTGAAGG | + | 6.33 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_01566 | chr2:238568879-238571154 | Aorta | SE_01566 | chr2:238571303-238573686 | Aorta | SE_23331 | chr2:238571349-238572688 | Colon_Crypt_1 | SE_23963 | chr2:238571497-238572221 | Colon_Crypt_2 | SE_24998 | chr2:238570520-238573269 | Colon_Crypt_3 | SE_25815 | chr2:238570466-238572445 | Duodenum_Smooth_Muscle | SE_26722 | chr2:238570190-238571204 | Esophagus | SE_26722 | chr2:238571408-238572780 | Esophagus | SE_29646 | chr2:238570702-238573032 | Fetal_Muscle | SE_31908 | chr2:238568844-238571159 | Gastric | SE_31908 | chr2:238571335-238571973 | Gastric | SE_31908 | chr2:238572010-238572953 | Gastric | SE_40633 | chr2:238570413-238573764 | Left_Ventricle | SE_42111 | chr2:238568829-238571135 | Lung | SE_42111 | chr2:238571181-238573276 | Lung | SE_44921 | chr2:238570901-238572414 | NHLF | SE_45786 | chr2:238570567-238572579 | Osteoblasts | SE_48071 | chr2:238568749-238573479 | Psoas_Muscle | SE_48757 | chr2:238572029-238573322 | Right_Atrium | SE_49604 | chr2:238572197-238573233 | Right_Ventricle | SE_51094 | chr2:238569466-238573270 | Skeletal_Muscle | SE_54582 | chr2:238569703-238573611 | Stomach_Smooth_Muscle | SE_58523 | chr2:238563966-238621920 | Ly1 | SE_59868 | chr2:238570692-238624050 | Ly4 | SE_65656 | chr2:238570576-238573536 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr2 | 238571237 | 238571811 | chr2 | 238572069 | 238572172 | chr2 | 238572122 | 238572400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I237660 | chr2 | 238568862 | 238573173 |
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Enhancer Sequence | ATGAGGGCCC ACCCTAATCT AGTACGACCT CATCTTAACT TGATTGTACA CGCAAAAAGC 60 CTATGTCCAA ATAAGGCCCC ATCCACGGGT TCTGGGTGGA CATGAACTTT TGGGGGATGT 120 TACTGAACGC AGTGCAGGGT TCTTACATTC TCACCATCAC GTATATGATT TTATTCTTCA 180 GGGTGCTAAG GTGTGGTGTG TGCCATGTGC TCTTAACCCC TTAGAAAAGA TAAGGACAAT 240 TTTTTTTTCA GGTCCAATGT CTGAATGTAT TTTTTTTCTT TCTCTTAGGA TTTGAAGATA 300 TATAACAATA TGTCATAAAC TGACCTGAAA TCCTTGTTTG TTCCGCAGCG AAATCCATTA 360 ATAATCCCTA TAACTGGGAC AGTTTTATGT TCCCATTCTC GGTGTGGCTA TTTATAGTGA 420 AACCTCACTT TCCCTGTGTT GGTTAACATT AAAAACTGGA ACTGCTTCTG AGGTAGGAGG 480 CGGGACTTGA CTCCAGAGGC GGGGCTTGGA CACTGGGCCA GATTGAGGAC TAGCTAAAAC 540 AGGCCCGGTG GGGAAAGCAG TCTTCAATCA GACACGCCCA CCAGCGCTAT GTCAATTTAC 600 CGTTGCCATG ACGGCACCCA GGCATTACCG CTCCTTTCCA CGGCAATGAC CCAGTGATTA 660 CTACCTCTTC CTTGCATAAA CCGCTCCTTA ATCTGCATGC AATTACAAGT GAGTATAAAC 720 AGGACTGCAA AACTGCCCTG AGGTGCTGCT CTCTGCCTGC GGGGTAGCCC TGCCCTGCGG 780 GAGCCGGCAG GGAGCTGGAA CACTGACACT TCAGTAAAGC TGTTTTCTTC TACCTATGAC 840 TTGCCCTTGA ATTCTTTCCT GAGCAAGGCC AAGAACCCAG ATGGGCTAAG CTCCACTTTA 900 GGGCTCGCCT GCCCTGCATC AGTTTAACTA AACTATTAGA ATTTTTAGTT TAAAAGAAAT 960 GAGTAAGATT GTGAGCATTC TGTGAGATGC GGAGTGAAAG AAGGTGCTGT AGTCTGAACG 1020 TTTGTGTCTC CCCTAAATTC ATGTATAGAA ATCCTAACCA CCAAGCTGAC TGTATTAGGA 1080 GGTGGGAGCT TTTAGGAGGT GATTAGGGCA TGAGAGTAAA TGAGATTAGT GCCCTTATAA 1140 AACAAACCCG GGGAGTTCTT TCCCCCCCCA TCCCGCCATG TGAGGACACA ATGGGAAGGG 1200 GGCCCTCACC CCTTCTATGA ACAAGAAAGG GGGCCCTCCC CAGACACTGA ATCTGCTGGC 1260 ACCTTGATCT TGGGCTTCAC AGCCTCTGGA ACTGGGGGAA GTTAATTTCT GTTGTTTATA 1320 AGCCACCTAG TCTATGCCCT TCTGCTACAG CAGCCTAAAC AGCTCAGCCT TAATGGACGA 1380 GGCACATGGA ATGACTTCCG GGCCTCTGAC AGGGTGCTTG GGGAGGATGG TGTGATGTTG 1440 CGTTATCACT CACAGACACT GTGGAACTGA CTGGGTTGGT GGAGCGGGGA CCCGGGGAAG 1500 AGTTCAGTTC TGTTCTGGGA ATGTTGCCTT GAGGCAGCTG AGCACTACCC ACAGGGAAAG 1560 GTCTGGCAAA GGTTCACGTG CATTCGCCTG GGCCATAGGG GAGAGGGGAG CCGTCAGCGG 1620 TCAGGGTGGT CAAAGCCACA TAGTTGCATG AGGTCTCCTA AGTAGGTCAG TGGAGCAGAG 1680 TACCCAGGGT GGAGCCCCGG GAACCTCAGA AACAAGGAAG GGGTGAGCAG AGGAAGGGTC 1740 GCCCTCAGGG CACTGGGAGG GAGGAGCAGG GTGAAGGGTG GGGGCAGAGG GGAAACAGCC 1800 ATGTCCATGC TGCAGAGAGA CCCAAGGGAG ACCCGGGGAA GAATGTCACT TGCACCTTGC 1860 AAAAGGGAGG GTCCTGGCGG CCTCAGCCAG AGCCGTTTTA GTGAAGTCAT GGGGAGAAGG 1920 ACCACAGAGG CTTAGTCCTG GCTGGGGCCG CAGTGGGACT GGCAGTGGAG AGGAGGGGGC 1980 CCAAGCCAGG GAGATTGAGT TCTTGGCAAA GAGGCCGGCG GCGTTCTCCA CTGCGTTTCC 2040 ATCCGCAGGT GCGCCTGCCG CCTGGCCTGT CCACAGTGTG CTGGTTGCTG GTATTCAGTT 2100 CTGGATTGTA CCTCTGACTG GACTGAGGTC 2130
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