| Tag | Content |
|---|
EnhancerAtlas ID | HS116-02754 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr1:203640580-203643850 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr1:203642872-203642885 | AGCAGCTGCCCCT | + | 6.18 | | RFX5 | MA0510.2 | chr1:203641599-203641615 | CTTTGCCATAGCAACC | + | 6.15 | | RFX5 | MA0510.2 | chr1:203641599-203641615 | CTTTGCCATAGCAACC | - | 6.32 | | Stat4 | MA0518.1 | chr1:203642667-203642681 | CTTCCAGGAAATAA | + | 6.57 |
|
| | Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
| SE_00067 | chr1:203629585-203648819 | Adipose_Nuclei | | SE_02128 | chr1:203640353-203643870 | Aorta | | SE_12116 | chr1:203640923-203646594 | CD3 | | SE_13787 | chr1:203639960-203647614 | CD34_Primary_RO01536 | | SE_14468 | chr1:203640936-203646834 | CD4_Memory_Primary_7pool | | SE_18521 | chr1:203639600-203646936 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19166 | chr1:203639152-203646704 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20327 | chr1:203640357-203646733 | CD56 | | SE_22546 | chr1:203639536-203646747 | CD8_primiary | | SE_25804 | chr1:203639346-203646040 | Duodenum_Smooth_Muscle | | SE_26726 | chr1:203640282-203641476 | Esophagus | | SE_26726 | chr1:203641519-203646078 | Esophagus | | SE_29679 | chr1:203639748-203645291 | Fetal_Muscle | | SE_36167 | chr1:203641378-203643905 | HMEC | | SE_39762 | chr1:203639598-203643774 | Jurkat | | SE_40816 | chr1:203640451-203643887 | Left_Ventricle | | SE_42264 | chr1:203640417-203643863 | Lung | | SE_44861 | chr1:203640389-203643779 | NHLF | | SE_45901 | chr1:203638689-203645287 | Osteoblasts | | SE_48668 | chr1:203640299-203643783 | Right_Atrium | | SE_53094 | chr1:203640491-203643860 | Small_Intestine | | SE_54514 | chr1:203628856-203647840 | Stomach_Smooth_Muscle | | SE_66630 | chr1:203639598-203643774 | Jurkat |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 203643182 | 203643803 | | chr1 | 203641153 | 203643812 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I203669 | chr1 | 203638729 | 203646707 |
|
Enhancer Sequence | ACCTGCCTCT CCTGCCCATC TTGAACCACC TATGGCCCTT ATTTCTCTTC TTCTTTGCTA 60
TTTTATTTTT GGTTGAGGGA GTCAAGGCAG AGGGCCATAG TACTTCCATC GAATAGATGC 120
AGACTGACCT CTGATCACTC CCTAACCCCT CGGCCAAAAA CCTTTCCCAC GTCTCTGGTG 180
CCCGAGACAT ATGTGTCTAG GGAGGAATCA GCTGCACTGT TACTCATCCA TCAGCATCTG 240
AACCTTGCAT GCTGACTCTG TGATGCTGAC TAAGGGTCCT CACCACCTTG ACTAAAATCT 300
TGGGTCTTGC TATGCAGAAG TAGCCCTTCA CCCCAAAGCT AAGGAGAAAG GATTGGATGA 360
AAGTTCTCTG TAGAAGTGGA GGAAACACGT GTCTCCTCAG AGGTACCTCT AGAGGTTGTT 420
CTCTGCAACC CTCCAGCTAG AGTGAGCAGG CTCCTTGCCT GGGTGGCACT GCTACCCACA 480
GAGGGGATGG GGGCTTCGAA GCTCTCCTCC CACGACACCT GGTGAATCCT CCATGTCTTC 540
CTCCCTTGAT AGTGGCAGCT GGTGGGGGCT GGGGGGAGGG AGGAGTGCTG CTGTTAGAGC 600
AAGAAGACAA AGTGGCTTTG TCTCTTATCC GTAATATAAG TGCAGGGAGG TGAGAAGACC 660
CTGGGGTTTG GCGTTTCTCC TTGAGGAGCT GAGCCAGAGG CAGGGCTTTG GTTCCTAAGT 720
GATTAGAGGC CTGCATGGCC AGAGGCCGCA CCTTCCCTTT TGGAAAGGAG CTCACCCACA 780
CTCCTTGCTT CCATCTTCCC CTTCCTGGCT CAAGTCATAG GCTCTATTTT CTGGCTATCC 840
TGTTTTTGTT CCTGAGTAAG TTGCGGTGGC TCTTTTTTTT TTTTTTTTTT TTTTTTTTTT 900
TTTTAAAGCT GATTTAGGGG GTTGGGAAAA GAAAACTTTA AAAGTAAAAT AATAAAAAAC 960
AGACCACTCT GTCATTACAG GCACATAAAT AGCTTTACCG TCGCTGGGCT GCACACTCGC 1020
TTTGCCATAG CAACCTAAAG CGACTGTTTA TAACAGCTTG TCAACTGGCC TGGAAACCAG 1080
CAGCTGCTGC TGGCCGCCCT GGCCTCGGAG CAGTGGGCAG GCGCTCCCTG AGAGGTGTTA 1140
TGGAGGCGGT GAGCCTGGTG CTTCTTCTGG AACCGTGGGG GATGGCAGGG GAACGGCAGC 1200
CTGGGTTCCA GAGGCAACCA GGGGCAGTAA TGTTTTGGGA GCCAAAGTGA GCAGCGAATG 1260
TCTTTTGTTT TTGTTTTCCC CTCATCTGTG TATGGGCCCC AGCATCGCTC ATCTCCTGTG 1320
GAGATAGAAG ACAGGGCTGG GAGGGGATTT GCTCCACTGG AACCTGAAAG GGGCCTGGGT 1380
GTCCCTCTGA ACCTCACGAG GTGGCTTGTT TTAACTTTTC GAATAGACCT TGGCTTCTGT 1440
TGTAGCCTGT TGAGTGACAT CCTCTCAAGT CTGTTTTCTC AAAGACTAAA AAAATGTGGG 1500
CTTTTTCAGG GCTCTGTCTG GGAAAGGGGG CTGCCCAGAG ATAAATGGAA GCAGAGATCA 1560
GCAACCTGGA AGGACTAGCA GAGGGAGAGG GAAGAGTGAA GGAGACACAT GGCAAGATCT 1620
TCCTGTGCCT TCCCATGTCA GCCTGGAGCT GAAGGGGTTC ATGGGAATGC TTTGGAACCT 1680
CGCAACATTT TCAAAGTGTG GTCCCCAGAC CAGATGCATC AGCTCACCCT GTTAAGGAAC 1740
TTGTTAGGAG TGCACCTTCC CAGGCCCCAC CTCCGTTCTT GTGCACCAGA AACTCAGGAG 1800
TTGGCAGGGA GGGGCCCAAT AGGTTTGCCC CAGTTCTCCA GAGGATCCTA GTGCTCACTC 1860
TGGGTTTGAG AACCACAGCT CTAAAACATT ACTCAAGTGC AAGGAAGCAT GATCAGTTCG 1920
CTTTCCAAAG GCCTAGGCTG ACTGAATGGA TCCTGTCTGT GCAATATGTG AACAAGGAAG 1980
AATAAAACAG GCGCAGAGGG GTGGCAGGTT ATTAGCGATC ATTCCTGGCC ACCTTTTTTA 2040
ATAAGCACTG TCTTTTCAGC ATGGAGCCCT CGCTGATTTG CCTGTGACTT CCAGGAAATA 2100
AGCCCAGAGA AGGCTGGAAT AGGTAAAGCG GGGATGGGAG GTTCTCTGTA CTCTGTACAG 2160
GTGAGACTGT CAGAGTGGAG AAAGGGAATG GGAGCAGCCA GGCCTGATGA CCAGTATGGG 2220
ACATGCTGAC TAGTATCTGG GCCACACAGG AATGTTGTTT TAAGTCCTCT CCTGCTGAGC 2280
GTCTGGGGAC AGAGCAGCTG CCCCTGGTGC TCCCTTTTGG TGGATGAGAT GTGGCCTCCT 2340
CAGTCTGTGG CCAGGCAACT TCTTCCCCCT TGTCCTGAGG ACTCCACCAG ATCCTGAGGC 2400
CTGGGAACAA CCAGGTCCCG ACCCGGTAGC CCAGGGAGAT GACCCCTCTC CATAAGCATG 2460
ACATGATTCT GCTGAAATTC GTTTCTAAAA ATAACCTAGG ATCCGATCCA GCTGCTAAAA 2520
AGCCCCTTTG TTCCCTTGAA ACCAAAATAT GGAAAGCCAC AGCAGCCCCA AGAAAGACAG 2580
TCTGTGTAGT CCAAGAGAGT GCATATACGA AATACTTGAA TGCTGCTGCC GGAGGGCTGC 2640
GTCCTGTCTG TGGCCTAGAA GCTTCCTGCC GCAGCTCTGA GGAGTGAGTA GCAGTTATCG 2700
TTGCTAACCC TTATCCTGAG TGAACGGGGT CAGGAGAGGC TGCCAGTACC CCTTTTGTTA 2760
AACAGACCTT CCAGATGGCA TTGTCACTTC CACCTGAAGG TGGCTCTTGT CCTCCTTAAA 2820
CAACTGAAGG AAATGGTGAG CGCTGCTGTT TCATCCTCTA CATTTTTTTG AGCTCTAGCT 2880
TGCTGTGAAC ACCCCTACCT CCACCCCATA CATCCTCTGA GTCACTGGAG GACACAGAGG 2940
TGACCCAGGC CAGTGTGACT CACACAATTT GAAAGAGGTT GGCTTTCCCA AGGCTCTGGG 3000
CCTAAGGGAC TGCCCTTTCT CATCTTGATA ATTTTTTTTG AGATGGAGTT TTACTCTGTT 3060
ACCCAGGCTG GAATGCAGTG GCACGATCTC AGCTCACTGC AACCTCTGCC TCCAAGGTTC 3120
AAGTGATTCT CCTGTCTCAG CCTTCTGTGC AGCTGGGATC ACAGGCGTGC AACACCACAC 3180
CTGGCTTTTT TTTTTTTTTT TTTTTTTTTT TTTTTTTTTT CTGAGATGGG GTCTCACTGT 3240
GTCTCCCAGG CTGGAGTGCA ATGGCACAGT 3270
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