| Tag | Content |
|---|
EnhancerAtlas ID | HS053-00593 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:22281600-22284810 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr1:22283664-22283675 | GCTTCCCGCCC | - | 6.02 | | EWSR1-FLI1 | MA0149.1 | chr1:22283831-22283849 | GGAAGGTAGGACGGCAAG | + | 6.16 | | EWSR1-FLI1 | MA0149.1 | chr1:22284265-22284283 | CCTTTCAACCTTCCTTCC | - | 6.53 | | HES2 | MA0616.2 | chr1:22284333-22284343 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr1:22284333-22284343 | GGCACGTGCC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr1:22284410-22284425 | TGAACTCGTGACCTC | - | 6.12 | | STAT3 | MA0144.2 | chr1:22282028-22282039 | CTTCCCAGAAA | - | 6.02 | | TFAP2A | MA0003.3 | chr1:22283357-22283368 | AGCCTCAGGCA | + | 6.32 | | Zfx | MA0146.2 | chr1:22284435-22284449 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 16 | ID | Coordinate | Tissue/cell |
| SE_00032 | chr1:22280798-22286056 | Adipose_Nuclei | | SE_01556 | chr1:22281528-22284380 | Aorta | | SE_25801 | chr1:22281815-22284310 | Duodenum_Smooth_Muscle | | SE_26605 | chr1:22281524-22284310 | Esophagus | | SE_29681 | chr1:22281484-22283021 | Fetal_Muscle | | SE_29681 | chr1:22284382-22285187 | Fetal_Muscle | | SE_37945 | chr1:22282670-22286119 | HUVEC | | SE_40620 | chr1:22281477-22285092 | Left_Ventricle | | SE_42167 | chr1:22281597-22285044 | Lung | | SE_47476 | chr1:22282432-22282926 | Pancreas | | SE_47476 | chr1:22282944-22284257 | Pancreas | | SE_48565 | chr1:22281500-22284373 | Right_Atrium | | SE_53700 | chr1:22281497-22284094 | Spleen | | SE_53700 | chr1:22284246-22285468 | Spleen | | SE_54522 | chr1:22281743-22283438 | Stomach_Smooth_Muscle | | SE_65890 | chr1:22281595-22285391 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 22283005 | 22284245 | | chr1 | 22281632 | 22282689 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I021955 | chr1 | 22281644 | 22285107 |
|
Enhancer Sequence | GGCGTGAGCC ACCGCGCCCG GCCATACGAA GTTCTTTAGC AATAGAAACT CCTGTGCGGG 60
CCCGTCACAA TCCACAGTCC ACAGTCACTA GGAGTCTTTT GCCTGGGTTG GGTAGTTTCA 120
GCTGCTGAAA CAGGGAGCCA GGAGGAGGGA TCAGAAGGGC GGCCCGCAGC CAGCGGAAGA 180
GGAGTGCGAG GGAGCTCGGT GGACCAGGGA AGCGGTGTCC ACAGTTCCCT TGTGGGGCCT 240
GAGCCAGGGC TTGGTTCAGC TCTGGGTGGG GGGGCCGGGT GGGCAGGCAC CCAGCAAGAG 300
GGCTGGGCCT CTCTAGGATG CTTGTCCCGA AGGTCCCAGG CATCGAGATC ACTACCCATT 360
TCTGGCCTAA GAGGCACTGG AAATAGCTCT AGGACAATTA TTTCAGGAAG AATGTGCTAT 420
TCCTCCATCT TCCCAGAAAG CCAGGCTGTG TCCTAGATCA GGACAGTCCC TCTGCAGCCT 480
CCCACCTCAG GGGAACCTCC AGCCCCACTG AAGGCCCCAG AGGCCTTCAG AGCCAGAAGG 540
GGCTGGGAGT CAAGAGTGGG AAGTGAGAGG CCCCTTTCCT GGTGGGGGAG GGGAAGTTCT 600
GGCCTTCGAT CCTGGGCTCT TAGGGCCCAG GCTGGAGTTA GGCTGGGCCG GCTGGAGTCC 660
AGCTGACTCC AAGCCCGGGG CGCATGATGG GAAGGATATG GGGAAGAGGT CTGCCCCACC 720
TCTTTCCTAG GCTCAACCCT GGGAAGCTGA TATTTGTGAG GCATATATCA TGTGCCATAG 780
AACATGATAT TGTGGGTCCC AGGCCCTTCT CAGCCTCCTT CCCTCCCATT TAATCCTCAC 840
AGCACCCCTA AGAGGTATTT TGTTTTCCAG ATGAGGTAAT CGAGGCTCAG AGAAGGCTAG 900
AGACTTGCCC AAGCTTGCCC AGGAGGCTTG AGTGAGAACC TGGCCTTCTT AAGTGCAAAA 960
GAGGGTAGGC TGTCCCTCCC ACTCGGTGAG GACTCAGGAA GTGGCCCTGT GAACTGAGTA 1020
GCACTGGGAG GGGTCTAGTC TGGAGACCCA GGATGTTGGA CAGCAACAGT CCCATCCCCC 1080
ACTCGCCCCA TTCTCCACTC CCCAGCCAAG CCCAGCTGCC CCCGCTTCCA GCGCTGCAGA 1140
GAAGATGCAG AGTCTCAGAA GGTCCTGGGT GGTGGGGTGC CCTGTCCTGC CATCTCCAGC 1200
CACAGTGGTA CCCGCTGCCC CACCTGGCCC CTCTCCACCA CCTCCAGCAT TGGATCCTTG 1260
GCTTCATTGC CAAGGATAAA CTGGCTGAAA AGTAGCTCTG CATCATCCGT TGCCCTCCCC 1320
CTGCACCCAC CCCCAACCGG CTCTCCTCAT TCTCACCTAT CCCCCCTCCC ACCCACCAAG 1380
GGCCACAGTC CCACCAACAT CCTCTGCCCA TCCTGTGCTC ACCAAGAACA CTAGGGGCCC 1440
TTCCCCAACC CCAAGCACAG AAGTTCCAAG GCATCTCATT CTCTGTGCTC CCCTGGGTAG 1500
GGGGAGCAGC TCCCTTCTCC AGAGACCTGA GGACCCTGAC CCATTAGCAC AGGTGCTGCC 1560
CATTAAGCCT TCACCTGCCG CTCAGCAGTT TCTCTCCTTC CCTGGGGCCT GAGAGAGTGG 1620
GAAGTGCCCC CTTATCCCTT CAGCCACATG GCTCTTATAA GCCCAGCTCA GCAGCCACAT 1680
GTTTGTGACA CCCAGGTCAG TTCAGGGGAC AGCTAGAGCC AAGAGCCCTC CACCCTGCCC 1740
GAAGGGCATC TGTGTCCAGC CTCAGGCAAC TGTTGGCACT GTGTCCTGAG CCTATACCTG 1800
GCCTTGAGCC AACTTGCCTG CCAGACTGGA AAATCTCTCC TGGGCCTGGA CCTGGCCCTC 1860
CCCCGGCTGC AGCCTTATAC CCACCAGAGC ACAATGAGTC ACGCGTCCTC CTCACCTAAC 1920
ACCCTCAAGG ATATGGGGCC CCTGCTCACC CACTGCCAAA AACAGCACTT CCCCAAGTCC 1980
ACATGTGGCA GGCACAAGCC AGGGCAGATC TGAGCTCAGG AGCACTGGGC AGGAGTGTCT 2040
TGGCAGGAGT CCCTGCCAGG GAGAGCTTCC CGCCCGCCAA GCTACCTGAG GGCTTTGCAG 2100
GTAGAGCAGC CAATCTGGGA GGCAGCAGGG CTCCCATCTT GATGGGGCCC GGGAAAGTCC 2160
CTGTAAGGAG GGTGCAGGAG GACGGTCACA GGCAGGCTTA TGTACAACCT TGCTGAGAGA 2220
ACAGCGCCCA CGGAAGGTAG GACGGCAAGT AAGAGGCTTG TGCTGTGACC TGGGGCAAAC 2280
AGGTGAACTT CTCCAAACCT CAATCTCCTG TTCTGTGAAG TGGAGGTGGG GAGGGGACTT 2340
CCGGAACACT GTTGACTTGA CTGGCTCGCA ATCACAGCGA GTGTTCACAA CGTGCTCCCC 2400
GTGTCCCAGG CACACTTCCG AGTGCTTGAT TACCTTACGA GTGGCTGCAG CCGTGTGCTG 2460
GCCCACAAGA GCCAACTGTT AAATGTTCTG AAATGTGGTG AATGGTTGTT AAAACACAGG 2520
TAGCTTGAAA TCAGCCATAA GGAAAATATT TGGACGACAG GAATTGGCAG ATATGACACA 2580
TTAGGACTTG TTGCTGTTGT TGTTGTTGTT TTGAGACCGA GTCTCCCAGG CTGGAGTGCA 2640
GTGGTGCAAT CTCGGCTCAC TTCAGCCTTT CAACCTTCCT TCCCAGGTTC AAGTGATTCT 2700
CCTCCCTCAG CCTCCCGAGT AGCTGGGATT ACAGGCACGT GCCACCACAC CCAGCTAACT 2760
TTTGTATTTT TGGTAGAGAT GGGGTTTCAC CATGTTGACC AGGCTGGTCT TGAACTCGTG 2820
ACCTCAAATG ATCCGCCCGC CTCGGCCTCC CAAAGTGCTG GGTTTACAGG CATGAGCCAC 2880
CGCGCCCAGC CCCTTTCCTT TAATCGTCAG ATATAATGGC TCAAGTCTCC ATCCCGCGGG 2940
CTGTGGGAAG TCCAGAGCCT TCCCTGCTAT TTTTCAAGGA GCCCAGAAGG CTGTTATGGC 3000
CTTTTGTCAC CCCTCACTCG GAATCTCTGC TTCTGGGTCA GTGTTCAGCC CCTCTTGCTG 3060
CCCCACCTTC TGTGACTGTC ATGTTCTGTC AGCAAAGTCG CAGCCCCTGC CACACTGCTC 3120
TGTGACTGCT ACTCCACAGG AGACCTTTCT CCAGCTTCTC TCTTCCGCCT GCCCCTGTTG 3180
CGTGGCTCCC ACTGCCCCCG TAGTCCTCCC 3210
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