| Tag | Content |
|---|
EnhancerAtlas ID | HS092-28395 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr3:58035930-58039270 |
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 | ATTTTTAGTA CAGACGGGGT TTCACCATGT TGGCCAGGAC GGTCTTGAGC TCTTGACCTC 60
GTTATCCACC CGCCTCGGCC TCCCAAAGTG CTGGGATTAC AGGCGTGAGC CACCATGCCT 120
GGTCTCTTTT TCATTTTTAA AGGGTAATTT GCTGTGCAGG AGTGGGCTCT CAGACCAGAA 180
GTGGGGACCT GAATGAAATC AAGGACTGAG TATGGTAACT ACAGCCATTT AATTTTATTT 240
GAAGTCTCCC GTAAAATGTT CTGGAAAAAA CAGGGGTTCC AGGGCTGGGT GGGCAGTTTC 300
AATCATGGAC TGGATTTTGT GGTTCAGATT TCTCTGGGCC TGTTGGAGGT TCCCCTTAAG 360
CAATTACCCA AGGCAGTTCT GCCCAGCTGA AGTACTGATT ACCTGCACAC TATACCAGTG 420
AGGACTCATG GGTGAGCAGA TGGGAGGCAC TGAGCTTGAT TCTGAAACCC TGGCCTCCAT 480
CCCACCTGAC ATTCAATGTC AGATTAGAAT TTGGAAGACC CTAAGTCTCC AGATTGGTGC 540
ACTGGGTAGC TCCTGAAATG GGGTGGCTGA GACAGGTCCT CTGTGCCCCC TTCCACAGCT 600
TCCTCTGGGG CCCTTCTGCT CACTGGCATG TGCTTCTGGG CAAATAGGCC TCTCCCAGCA 660
TTTGTTTTGG CTCTGTGAAA TGGGGTAATA TTTGTTCCTA TTGCGGGTGA AGCGCTGCTG 720
TTGGGATGCT CAGGTAACTC ACTCCGTGGG TAGCTGATAT TGCCTGGGCA AGTGGCATTT 780
TAGAGGAAAT CTGTGCCATC AAAAGAGTTG GACCTGATCA CACTTTTGCT TTTGAATATG 840
CTTTGTCCCA GCCTGGCCAT TCGTCACTTG GGACCCCCTG AGTCTCTCTG ACCCCACTGT 900
AAAATGGATA TGCCATGGAG TTGTCCCAGG AATCAAGGGC AGGTCCTCTC CAGTGAGTGA 960
TGGGCTTGCC TCTCACTTCT CTAACACCCT TCTGCTTCCT TGTGTAAGAT TTCACTATTA 1020
GTGGCTATTC TCTTTTACAG AAGAAAAAGG GAGACGCATG CCTCTTCCAG TTCACTGTTC 1080
ACCATTGCAG CATATTTATT CCAAGGGACT GGCCGAATCA TCCCTTTCTT TGTTAGAATG 1140
TGGTTTTGTT GCCTTGAGAC AAGTGGCCCG CATGTCTGCA CTGAAGGAGG CTTTGCGCAA 1200
TAGCCTTGGG CACCTCCGGT TCTGCAAGCA TGTACAGTAC TTGCTCTCCT TTCCCTTTCT 1260
TTGTATACTT TTTCTGGTCT GCTACGTGTC CATCTGCATG TGGATAAAGG GTCGTCGTCT 1320
TGAGTAGTGA TTTTGCTGTG ATGTGATTCC TGTGAGGTCT AGTTGCACAC AGTGATTCCG 1380
AAGGTAGACC CAGCTGGAAA GCTTTTAAAT TGCTGATACT CCAGCCCCAC TCCCCAAGAG 1440
ATGCTGATTT TGTTTTGTTT TGGGGAGGGC AGTTTTTTTG GGTTTTTTTT TTAAGCTTTT 1500
TGATGTGTAG CCAGGGTTGA GACTGAAGTG ATTTTTGTGA GTAACGGAGA AGTGTTAAGG 1560
CTTGAGAAGT TGGAAGAGCC ATGCTTGAGA TAGGACCAAG GTCATATCCC CGGCATTAGC 1620
ACAGAGCAAC CCTGACCTGT TGGAGAGTTG GGCTGGATGG ATGCGGTCAG GGGAGAGACT 1680
CGCTTTATTT TATTTATTTA GAGATACAGT TTCACTCTTG TCACCCAGGC TGGAGTGTAA 1740
TGGCACGATC TCGGCTCACT GCAACCTCTG CCTCCTGGGT TCAAGTGATT CTCGTGCCTC 1800
AGCCTCCTGA GTGGCTGGGA CTCCAGGCAC GCGCCGCCAC ACCCTGCTAG TTTTTGTGTT 1860
TTTACTAGAG ACAGGGTTTC ACCATTGTTG GCCAGGCTGG TCTTGAACTC CTGACCTCAG 1920
GTGATCCGCC CACCTCGGCC TACCAAAGTG CTGGGATTAT GGGTGTGAGC CACTGTGCCC 1980
AGCCTCGACT CGCTTTATTA TATCCACACT TGGAATACAA TTCGGATTGA TTGTAGTGGG 2040
GCATTTTATA ATTAGGAAAA ATTAATCAGG AAAAATCACT CCATGTAGAT TAGTACCACC 2100
ATATGAGGGG ACAAGAATTT CTTCAGATTA GGAACTTCTT CCAACAGGAC TGACAGGGTC 2160
CAAAACTACT CTTGGATCCA GCTTTAAGAT GGACCCAGCC CACTGTTGAG TCCCCTCTGA 2220
GGTCTTCTCT CTGTGGATGG ATTTGATTGT TAACAATGGC TGAGTCATGT GGCACCCAGC 2280
CCGGTGAGTA AGACAGCTGA GTAAGAGGGG AAACAGGGCC TTTGGTCAGA AAAACCAGAC 2340
TGACTTCAGT CTTATCTGTT TAGAGAAGCC CCAGAAGCTG CAAAAATTGC AGCTTCCAGA 2400
CTTTAGTGTG CCGTGGTCAT GACATCGGTG TGGATGGCAG GTTGTCATCT GAGCAGTCAG 2460
GGTGGCAGCA CACAGCTTGC GGGCTGGCTG ATGGCCGAGG TGTGTGAACT GACCTGCCCC 2520
AAGTGACTTC AGTGCTGGGC ACAGCATAGG AGCAGTACTA ATGATATGGA CAGTATGCTC 2580
AGAGGACGTT AGGGAGCACA GCTTTGTGTA AAGGGCATGC CCTGCCCTGT CCGGATTTAA 2640
AGCAGCTATA GCACTGAAAC CCCATGGTCA CCCTCGCATT TCTACACTTC TGCCTGTGCC 2700
AAGTCTAGTT TGTGTGCCTC CTCCATTTTG TGTGTACATG GGGGTATTTT TTTCTGCTAG 2760
GCAACTGCTA TTTATGCCTC TCAGTACTGT ACTTAGTGTG TACCATTCCT GCAAGGTATA 2820
GACATTGTCA GCCCATTTTA CAGATGAGGA AAATGGAGTT TTTGAGAGGG TGAGATCATT 2880
CAGTGGCAGA ATGGAATGTT AACCCAGGTA GTCTAACCTC TCTGCTGTAG ATCTGATGTC 2940
CATTTGAACT TTAGACTTCC CATCTGTGTC TACAGTCTAG CCCTTAAAAA ATGTGATAAA 3000
CAGGTTTTTA GGTAAGTCTG TTAATTTCAG AAAGACATTA TTATTATTTT TTAGAAAGTT 3060
AGAGCTTATG TTAGGGCTCA GTCTATCCTC CTGCCTCAGC TGCCTGAATA GCTGGGACTG 3120
CAGGCACATG CCACCATGCC TGGTTAATTT CTGTGGTATA CATCATTGAT TACTGAGAAG 3180
TCACAGTCCG TTGTTAAATA ACTGAGCTAT TCATAGCCAA ATCATTTTTA AAAACACAAA 3240
TATAAGCAAA AACAAAACAT TTATTTATTT ATTTATTGAG ACGGAGTCTC GCTGTCACCC 3300
GGGCTGGAGT GCAGTGGCGC TATCTCAGCT CACTGCAACC 3340
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