| Tag | Content |
|---|
EnhancerAtlas ID | HS116-23818 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr3:58035840-58038950 |
SNPs | | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr3:58037766-58037777 | CCACACCCTGC | + | 6.62 | | NFE2L1 | MA0089.2 | chr3:58038185-58038200 | ATGGCTGAGTCATGT | - | 6.2 | | Nr2f6(var.2) | MA0728.1 | chr3:58037833-58037848 | TGAACTCCTGACCTC | - | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr3:58035975-58035990 | TGAGCTCTTGACCTC | - | 7.23 | | Zfx | MA0146.2 | chr3:58035998-58036012 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
| SE_00762 | chr3:58032174-58039716 | Adipose_Nuclei | | SE_01957 | chr3:58036187-58037788 | Aorta | | SE_01957 | chr3:58037976-58039178 | Aorta | | SE_23194 | chr3:58038002-58038849 | Colon_Crypt_1 | | SE_26498 | chr3:58033363-58039459 | Duodenum_Smooth_Muscle | | SE_27681 | chr3:58033703-58037597 | Fetal_Intestine | | SE_27681 | chr3:58037756-58039153 | Fetal_Intestine | | SE_29426 | chr3:58033550-58039244 | Fetal_Intestine_Large | | SE_30574 | chr3:58036943-58038968 | Fetal_Muscle | | SE_36024 | chr3:58033449-58039332 | HMEC | | SE_37989 | chr3:58025669-58040227 | HUVEC | | SE_41579 | chr3:58036203-58037368 | LNCaP | | SE_41579 | chr3:58038029-58038806 | LNCaP | | SE_45969 | chr3:58032377-58039419 | Osteoblasts | | SE_47269 | chr3:58019885-58040171 | Panc1 | | SE_56289 | chr3:58032310-58039346 | u87 | | SE_64106 | chr3:58036259-58039158 | HSMM | | SE_65730 | chr3:58034390-58037100 | Pancreatic_islets | | SE_65730 | chr3:58037283-58039024 | Pancreatic_islets | | SE_67942 | chr3:58032310-58039346 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr3 | 58036837 | 58037638 | | chr3 | 58037994 | 58038685 | | chr3 | 58038147 | 58038335 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I058046 | chr3 | 58032437 | 58041425 |
|
Enhancer Sequence | CTGCCTCCCG GGTTCTAACA ATTCTCCTGC CTCAGCCTCT GGAGTAGCTG GGACTACAGC 60
CACGTGCCAC CACACCCAGC TAATTTTTGT ATTTTTAGTA CAGACGGGGT TTCACCATGT 120
TGGCCAGGAC GGTCTTGAGC TCTTGACCTC GTTATCCACC CGCCTCGGCC TCCCAAAGTG 180
CTGGGATTAC AGGCGTGAGC CACCATGCCT GGTCTCTTTT TCATTTTTAA AGGGTAATTT 240
GCTGTGCAGG AGTGGGCTCT CAGACCAGAA GTGGGGACCT GAATGAAATC AAGGACTGAG 300
TATGGTAACT ACAGCCATTT AATTTTATTT GAAGTCTCCC GTAAAATGTT CTGGAAAAAA 360
CAGGGGTTCC AGGGCTGGGT GGGCAGTTTC AATCATGGAC TGGATTTTGT GGTTCAGATT 420
TCTCTGGGCC TGTTGGAGGT TCCCCTTAAG CAATTACCCA AGGCAGTTCT GCCCAGCTGA 480
AGTACTGATT ACCTGCACAC TATACCAGTG AGGACTCATG GGTGAGCAGA TGGGAGGCAC 540
TGAGCTTGAT TCTGAAACCC TGGCCTCCAT CCCACCTGAC ATTCAATGTC AGATTAGAAT 600
TTGGAAGACC CTAAGTCTCC AGATTGGTGC ACTGGGTAGC TCCTGAAATG GGGTGGCTGA 660
GACAGGTCCT CTGTGCCCCC TTCCACAGCT TCCTCTGGGG CCCTTCTGCT CACTGGCATG 720
TGCTTCTGGG CAAATAGGCC TCTCCCAGCA TTTGTTTTGG CTCTGTGAAA TGGGGTAATA 780
TTTGTTCCTA TTGCGGGTGA AGCGCTGCTG TTGGGATGCT CAGGTAACTC ACTCCGTGGG 840
TAGCTGATAT TGCCTGGGCA AGTGGCATTT TAGAGGAAAT CTGTGCCATC AAAAGAGTTG 900
GACCTGATCA CACTTTTGCT TTTGAATATG CTTTGTCCCA GCCTGGCCAT TCGTCACTTG 960
GGACCCCCTG AGTCTCTCTG ACCCCACTGT AAAATGGATA TGCCATGGAG TTGTCCCAGG 1020
AATCAAGGGC AGGTCCTCTC CAGTGAGTGA TGGGCTTGCC TCTCACTTCT CTAACACCCT 1080
TCTGCTTCCT TGTGTAAGAT TTCACTATTA GTGGCTATTC TCTTTTACAG AAGAAAAAGG 1140
GAGACGCATG CCTCTTCCAG TTCACTGTTC ACCATTGCAG CATATTTATT CCAAGGGACT 1200
GGCCGAATCA TCCCTTTCTT TGTTAGAATG TGGTTTTGTT GCCTTGAGAC AAGTGGCCCG 1260
CATGTCTGCA CTGAAGGAGG CTTTGCGCAA TAGCCTTGGG CACCTCCGGT TCTGCAAGCA 1320
TGTACAGTAC TTGCTCTCCT TTCCCTTTCT TTGTATACTT TTTCTGGTCT GCTACGTGTC 1380
CATCTGCATG TGGATAAAGG GTCGTCGTCT TGAGTAGTGA TTTTGCTGTG ATGTGATTCC 1440
TGTGAGGTCT AGTTGCACAC AGTGATTCCG AAGGTAGACC CAGCTGGAAA GCTTTTAAAT 1500
TGCTGATACT CCAGCCCCAC TCCCCAAGAG ATGCTGATTT TGTTTTGTTT TGGGGAGGGC 1560
AGTTTTTTTG GGTTTTTTTT TTAAGCTTTT TGATGTGTAG CCAGGGTTGA GACTGAAGTG 1620
ATTTTTGTGA GTAACGGAGA AGTGTTAAGG CTTGAGAAGT TGGAAGAGCC ATGCTTGAGA 1680
TAGGACCAAG GTCATATCCC CGGCATTAGC ACAGAGCAAC CCTGACCTGT TGGAGAGTTG 1740
GGCTGGATGG ATGCGGTCAG GGGAGAGACT CGCTTTATTT TATTTATTTA GAGATACAGT 1800
TTCACTCTTG TCACCCAGGC TGGAGTGTAA TGGCACGATC TCGGCTCACT GCAACCTCTG 1860
CCTCCTGGGT TCAAGTGATT CTCGTGCCTC AGCCTCCTGA GTGGCTGGGA CTCCAGGCAC 1920
GCGCCGCCAC ACCCTGCTAG TTTTTGTGTT TTTACTAGAG ACAGGGTTTC ACCATTGTTG 1980
GCCAGGCTGG TCTTGAACTC CTGACCTCAG GTGATCCGCC CACCTCGGCC TACCAAAGTG 2040
CTGGGATTAT GGGTGTGAGC CACTGTGCCC AGCCTCGACT CGCTTTATTA TATCCACACT 2100
TGGAATACAA TTCGGATTGA TTGTAGTGGG GCATTTTATA ATTAGGAAAA ATTAATCAGG 2160
AAAAATCACT CCATGTAGAT TAGTACCACC ATATGAGGGG ACAAGAATTT CTTCAGATTA 2220
GGAACTTCTT CCAACAGGAC TGACAGGGTC CAAAACTACT CTTGGATCCA GCTTTAAGAT 2280
GGACCCAGCC CACTGTTGAG TCCCCTCTGA GGTCTTCTCT CTGTGGATGG ATTTGATTGT 2340
TAACAATGGC TGAGTCATGT GGCACCCAGC CCGGTGAGTA AGACAGCTGA GTAAGAGGGG 2400
AAACAGGGCC TTTGGTCAGA AAAACCAGAC TGACTTCAGT CTTATCTGTT TAGAGAAGCC 2460
CCAGAAGCTG CAAAAATTGC AGCTTCCAGA CTTTAGTGTG CCGTGGTCAT GACATCGGTG 2520
TGGATGGCAG GTTGTCATCT GAGCAGTCAG GGTGGCAGCA CACAGCTTGC GGGCTGGCTG 2580
ATGGCCGAGG TGTGTGAACT GACCTGCCCC AAGTGACTTC AGTGCTGGGC ACAGCATAGG 2640
AGCAGTACTA ATGATATGGA CAGTATGCTC AGAGGACGTT AGGGAGCACA GCTTTGTGTA 2700
AAGGGCATGC CCTGCCCTGT CCGGATTTAA AGCAGCTATA GCACTGAAAC CCCATGGTCA 2760
CCCTCGCATT TCTACACTTC TGCCTGTGCC AAGTCTAGTT TGTGTGCCTC CTCCATTTTG 2820
TGTGTACATG GGGGTATTTT TTTCTGCTAG GCAACTGCTA TTTATGCCTC TCAGTACTGT 2880
ACTTAGTGTG TACCATTCCT GCAAGGTATA GACATTGTCA GCCCATTTTA CAGATGAGGA 2940
AAATGGAGTT TTTGAGAGGG TGAGATCATT CAGTGGCAGA ATGGAATGTT AACCCAGGTA 3000
GTCTAACCTC TCTGCTGTAG ATCTGATGTC CATTTGAACT TTAGACTTCC CATCTGTGTC 3060
TACAGTCTAG CCCTTAAAAA ATGTGATAAA CAGGTTTTTA GGTAAGTCTG 3110
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