Tag | Content |
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EnhancerAtlas ID | HS020-26970 |
Organism | Homo sapiens |
Tissue/cell | CD34+ |
Coordinate | chr2:238570100-238572460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:238570110-238570128 | GACTCCCTCCTTCCTTCC | - | 6.31 | 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 |
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| Number of super-enhancer constituents: 27 | 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 | chr2:238569122-238570436 | Colon_Crypt_3 | 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 | chr2:238569477-238570566 | Pancreatic_islets | 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 | GCCCTCCCCA GACTCCCTCC TTCCTTCCAG ATGTGAGCAA ATCCCTTTCC TTCCACCTCG 60 CTCTCGGCCC CTGGTTCACC TTCTGTTCCT GCCCAGGGCA AACTGCCCTA TGTGCATCTC 120 TGTCCTCATC CATGAAACCA TCCTTGTCCT CACTGTCGAT GGAATTTTTC AGTGATACCT 180 AACATCTGTC CCAGAGCCAT GCACGTTCCG AAAGCACATT CCAGGGGGAC AGTTGTGTCC 240 CTGGTGCAAC ACGGGAGTGG GCACACATTC TCTGTGCTGT GCATGGGGAC AGCTCCAGGA 300 AGAGAGAGGG CACTGTTTTC CTGTTTCCTG AGTCAATCCG CTGTAGTTCT GTGGCCCAGC 360 TGAGTGGCAT AGGCTCTCCT GACCCAGGTA CCTATCAGCC CCCAAAATAG GTGTTGCCAT 420 GATTCCTTTG GACAAAATGT AAAATCTGGC TGAAGACTGA GTCCTCGTGC ACCTAGCGTG 480 ACCCATGACA GCATGCAGGT GTTGGTCTGT AGGGATGCCA TAACAAAGTG CCACAAACTG 540 GGTGACTTAA AATAACAGAA CTGTATTCTC TCACAGTTCC GGAGACCGGA AGTCCAAAGT 600 CGAGGTATTG GGCCAGGTGG GTTCCTTCTG GAGGCTCTGA GGGGAAGGTG TTCCAGGCGT 660 CTCTCCAGCT TCTGGTGCTG CTGGCAGCCC TCGGCCCTCT GGCTTGTAGA CACATCACAC 720 CAGGCTCTGC CTCCGTCTCC ACGTGGCCCC CTCCCTGGGT ATTTGTGTCT CTGTGTGCAA 780 ATTTCTGTTT CCTTATAAGA AAGTCATTGA ATGAGGGCCC ACCCTAATCT AGTACGACCT 840 CATCTTAACT TGATTGTACA CGCAAAAAGC CTATGTCCAA ATAAGGCCCC ATCCACGGGT 900 TCTGGGTGGA CATGAACTTT TGGGGGATGT TACTGAACGC AGTGCAGGGT TCTTACATTC 960 TCACCATCAC GTATATGATT TTATTCTTCA GGGTGCTAAG GTGTGGTGTG TGCCATGTGC 1020 TCTTAACCCC TTAGAAAAGA TAAGGACAAT TTTTTTTTCA GGTCCAATGT CTGAATGTAT 1080 TTTTTTTCTT TCTCTTAGGA TTTGAAGATA TATAACAATA TGTCATAAAC TGACCTGAAA 1140 TCCTTGTTTG TTCCGCAGCG AAATCCATTA ATAATCCCTA TAACTGGGAC AGTTTTATGT 1200 TCCCATTCTC GGTGTGGCTA TTTATAGTGA AACCTCACTT TCCCTGTGTT GGTTAACATT 1260 AAAAACTGGA ACTGCTTCTG AGGTAGGAGG CGGGACTTGA CTCCAGAGGC GGGGCTTGGA 1320 CACTGGGCCA GATTGAGGAC TAGCTAAAAC AGGCCCGGTG GGGAAAGCAG TCTTCAATCA 1380 GACACGCCCA CCAGCGCTAT GTCAATTTAC CGTTGCCATG ACGGCACCCA GGCATTACCG 1440 CTCCTTTCCA CGGCAATGAC CCAGTGATTA CTACCTCTTC CTTGCATAAA CCGCTCCTTA 1500 ATCTGCATGC AATTACAAGT GAGTATAAAC AGGACTGCAA AACTGCCCTG AGGTGCTGCT 1560 CTCTGCCTGC GGGGTAGCCC TGCCCTGCGG GAGCCGGCAG GGAGCTGGAA CACTGACACT 1620 TCAGTAAAGC TGTTTTCTTC TACCTATGAC TTGCCCTTGA ATTCTTTCCT GAGCAAGGCC 1680 AAGAACCCAG ATGGGCTAAG CTCCACTTTA GGGCTCGCCT GCCCTGCATC AGTTTAACTA 1740 AACTATTAGA ATTTTTAGTT TAAAAGAAAT GAGTAAGATT GTGAGCATTC TGTGAGATGC 1800 GGAGTGAAAG AAGGTGCTGT AGTCTGAACG TTTGTGTCTC CCCTAAATTC ATGTATAGAA 1860 ATCCTAACCA CCAAGCTGAC TGTATTAGGA GGTGGGAGCT TTTAGGAGGT GATTAGGGCA 1920 TGAGAGTAAA TGAGATTAGT GCCCTTATAA AACAAACCCG GGGAGTTCTT TCCCCCCCCA 1980 TCCCGCCATG TGAGGACACA ATGGGAAGGG GGCCCTCACC CCTTCTATGA ACAAGAAAGG 2040 GGGCCCTCCC CAGACACTGA ATCTGCTGGC ACCTTGATCT TGGGCTTCAC AGCCTCTGGA 2100 ACTGGGGGAA GTTAATTTCT GTTGTTTATA AGCCACCTAG TCTATGCCCT TCTGCTACAG 2160 CAGCCTAAAC AGCTCAGCCT TAATGGACGA GGCACATGGA ATGACTTCCG GGCCTCTGAC 2220 AGGGTGCTTG GGGAGGATGG TGTGATGTTG CGTTATCACT CACAGACACT GTGGAACTGA 2280 CTGGGTTGGT GGAGCGGGGA CCCGGGGAAG AGTTCAGTTC TGTTCTGGGA ATGTTGCCTT 2340 GAGGCAGCTG AGCACTACCC 2360
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