| Tag | Content |
|---|
EnhancerAtlas ID | HS082-07737 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr12:13323820-13328430 |
SNPs | | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:13325009-13325027 | CATTCCTCCCTTTCTCCC | - | 6.36 | | MEOX1 | MA0661.1 | chr12:13327383-13327393 | GTTAATTAGC | - | 6.02 | | NEUROG1 | MA0623.2 | chr12:13327546-13327556 | GACATATGTC | + | 6.02 | | NEUROG1 | MA0623.2 | chr12:13327546-13327556 | GACATATGTC | - | 6.02 | | NFAT5 | MA0606.1 | chr12:13326325-13326335 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr12:13326325-13326335 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr12:13326325-13326335 | AATGGAAAAT | - | 6.02 | | PBX1 | MA0070.1 | chr12:13327606-13327618 | TCATCAATCAAT | + | 6.44 | | PRDM1 | MA0508.2 | chr12:13327067-13327077 | GTGAAAGTGA | - | 6.02 | | RREB1 | MA0073.1 | chr12:13324509-13324529 | GGTAGGGTGGTGGTGGGTGG | - | 6.58 | | RREB1 | MA0073.1 | chr12:13324092-13324112 | TGGCAGTGGGTGGGTGGGGG | - | 7.51 | | RUNX1 | MA0002.2 | chr12:13326808-13326819 | AAACCACAGAA | - | 6.32 | | ZBTB18 | MA0698.1 | chr12:13326266-13326279 | CTTCCAGATGTGT | + | 6.16 | | ZNF263 | MA0528.1 | chr12:13325012-13325033 | TCCTCCCTTTCTCCCACCCTC | - | 6.02 | | ZNF263 | MA0528.1 | chr12:13323840-13323861 | GAGGGAAGAGGAAGGGAAGAG | + | 6.1 | | ZNF263 | MA0528.1 | chr12:13323828-13323849 | GGGGGAAGCGGAGAGGGAAGA | + | 6.33 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_00070 | chr12:13322001-13329284 | Adipose_Nuclei | | SE_02366 | chr12:13324113-13327858 | Astrocytes | | SE_26715 | chr12:13324024-13328761 | Esophagus | | SE_36302 | chr12:13324133-13329267 | HMEC | | SE_45692 | chr12:13323910-13328954 | Osteoblasts | | SE_55863 | chr12:13323889-13330257 | u87 | | SE_64909 | chr12:13324369-13329500 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr12 | 13324034 | 13324099 | | chr12 | 13324615 | 13327060 | | chr12 | 13325962 | 13326157 | | chr12 | 13326583 | 13326856 | | chr12 | 13327354 | 13327623 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I013171 | chr12 | 13324128 | 13329500 |
|
Enhancer Sequence | AGTGGGCAGG GGGAAGCGGA GAGGGAAGAG GAAGGGAAGA GACTGTTGCT TTGCATTTTA 60
AATCCCCTGC ACCTTAAAAA AATTAAATTA TGTGCATGAA TTACTTTGCA AAACTGTACA 120
TTTGTGTATC TTTTAAAAGG GTAAATAGGG CTTGTTTGGA AGATAAGCCA AAAGGGGAAT 180
GATAGTAATG TTCAAAGGGT GAGATGAGTT GGAAGTTCAT GGCCTGATAG GGAGTGGTGT 240
GATCTAGTGG CTGGACTCTA GGGAGGTTGT TTTGGCAGTG GGTGGGTGGG GGGAAGAGGG 300
GGAGCGGCTG GAGGTGACTC TGGAAAAGTG GGCTAAGGCA AGGCTGTGGA AAGCATTGAA 360
TGCCATGCTA AGAAGTTTGG AATTTCCTCT GTTGACCATG GGGAACTATG AAAAAAAGTT 420
TTGAGCAACA TGATTCCATC TGTGTTTCAG AGGAATCATC CTTATGGCAA AATGTGGTAG 480
GATTTGGAGT GTGGGAATGG CAGGAAGCGG GAAGGCCAGA TCAGAGATGG TTACAAGCTT 540
AAGGGACTCT TTAGGGTCCG AATTAAGGCT TTCAACCTCT GTAGAAAACT GAAGTTCCAT 600
AATTGCAACT TGAATCAAAA CTCTTCTACC ACTTTCCTCG CCCTCCTGTG GACTGGGGTG 660
TCCTCTGCCC AGGAAGACAC TGATGGGGCG GTAGGGTGGT GGTGGGTGGG CCACAGGGAA 720
CTGCCCACCC CTCCTCATTC AGGGGCCACT AGAACCTCCT GTCTGGTCCA AATCTCACTT 780
CAGATTTTTA GAATCTTACT ACAAACAATT TTTTGGCCAC ATTTCAAGAC ATGTCTTAGT 840
TTTTAGCACA GGATTTTTAC CAATCTCTCC CTAGCCCCCT CCACACCCTT TAATGATTCC 900
CTTGGTTTTT ATAAGTAGGT TTCCAGTTTT TTCCTCCTGC CTGCCAGCTC ATCTAAGAAG 960
TAGGATTTTT TTTCTCCTTT TTTATTATTG GTATTTAAAA AATAATAAAA TGGAAAAAAT 1020
GAATGTTTTT GCACTTCTGG CCTCTTGCTT TCGAGGTTCA CACCCACTGG CGCCCTCCCT 1080
CTGAGGCTCA CTAACATTCC ACACTGCTGG GCGTGTGTCT GTGTGACTAG GATTCCTTGG 1140
CTGTTGTCTC CTGTCATCAT AATTTCTCCC TTACCTCCTC ACCTACTTGC ATTCCTCCCT 1200
TTCTCCCACC CTCTGGTTGC CAGGCAACAC AGCTGAGGGG CAGGAGGAGC TGGCAGGCAG 1260
TGCCCCCATG GAAATACTGG CTGCCTGTCT TCCTCTCCCA GCAGCTTGGC TGGGAGTTGG 1320
GCAATTGCTG AAGGTCAAAG GCAGCCATCC ATAGTTGTGT CATTCCCTCC ACTAGGTATA 1380
AACCTGACAC AATCAGGGAA ATACTTGAAG GTAGGGAATG GGGTAAAGTA AGGCAGTTAG 1440
TTTTCCCTTC ACACCCAAGA GGCTGGCGTG ACTCCTGCCT TCCGGCAGAA GAGGGTAAAG 1500
GTGGAGATGA ATTGGCCTTT CTGCGTTTCA GAAATGTGAA TTTCATTTCC TTCCACACCT 1560
CTCTGTCCAG TGGCTGGGCT TGAGAATTAG AGTCGACCCG GCAAAATGAC AAATTCACTT 1620
GTTAGCAGAG GTTGAATTTT TTGAGTTGGG GCCCATTTCT CTAGTACCAA ACATGATCTG 1680
GGGACTCGCA GCATGGACAG CCTCTGGGAG CTTGTTAGGA ATGCAGACCT CAGTCCCATC 1740
CCAGACCACC GAAACAGAAG CTGTAGTTTT TCAGAATGAC TGGGTAATTT GCATGCATGC 1800
TGATCAAATA CTGTCGATTC GGTCTTGTGT TCTTGAGACT TCTTCCTTTC TCCTGCTCAG 1860
TGGGGCGTCA TGGAGTCCTA TGTTGGGGTC TTTCATGGGT TTACGGAGAG ATGAGTGAGC 1920
AAATGCAGAG ACTGTCTCAG CCTGACACAA ACCCCTTCCC CTTTCTCCAT CTATCCTTAC 1980
CCTACACAGG TATGAGACAA GGCATGTCCA GATATGTTAC CTCCCTTATC CTCACACACT 2040
CCTGTGTCTA TTTTTAAACA ACGAATCCCA ATTTTATTGA TGAAGAAATG ACCTAGGTTG 2100
TTGAAACTTA CAGAGCTTCA ATGGACTCGC CCTGGTGATT ACTGAACAGC TTGCTTTCAC 2160
CTTCCTTTGG TATGTGTCCT AGGCTAGAAA TTCTGTCCTT TTAAACACGT AGCTCCAAAG 2220
AGTCATTATT GAAAAAAAGC AATCAGAAAC AGAATGTTGG GTTTGGTTTG AGTCATAAAT 2280
TCCACCATGT AGGGATGAAA TTAAGGACTT TTTCCTGAGC CTCTGCAAAT GATTCCAGTA 2340
GTTCAGAGGC CCTTTTGAAC AAGAGGTTAC ATGGATTGGG TTTCAAAGAA AAGAATGTCG 2400
AAAGACATCT TCCAGCTGAG AATGGGCTCC AGATGTGAGC ATTGCTCTTC CAGATGTGTG 2460
GACGAATGGA GCGGGACTGA GATGCCTCAC ATGTCTGCAA CATGAAATGG AAAATCCTCT 2520
CTCAGCCACA GGGGAAAGTA GGACAGGGGG AAGACAAATG GAATCCAAGT TAAACTCTTC 2580
AAGGTGGGGC CAGACTAACT CTAAGAAATC ATTCCCAGGT GGGCTGATAT TTTACGTATG 2640
CAGTATGTGT AGAGGCCACA CCTCAAACTG TGCTGCTGAG CAGAAACTCA GAAGGTATTG 2700
TGTCTGCAGG AACTCACTCT TCTCAGACCT GCATAAATCT GATTCAGCCC CTTAGAGGAG 2760
CCTCACTGAG AACTGTTGAG ACTACAGGCA GATCAAGCAG GACAGGCGGC GAGACTTACT 2820
CAGCGGAGCT GAGAACAGAG CCCAGAATGC GGAAGGGGAA GGAGCCAGGA GTCACACAGT 2880
CCTTTCTTTC TTCAGCTTCT GAATCAGCAA CTCATTCTCT CGGGGATCGC TGGGTTTGTT 2940
TCTTTACAAT GGCTAGAAGG TCCCATGTTT CTCAGATGAG TAAATTTGAA ACCACAGAAA 3000
ACTGAGGCCT TGTGGCCAAG TCCTCTTGGT TTGTCACATC TCTGAAAATC TGAGCCATTG 3060
TCAAACTCCT GGCTGCAGGG AATTAAACCC TTTATTTCCC TCTGCCAGCA TCTTCACCTT 3120
CTCCAGGAAG ATCTGCCAAA GGACTGCTCC AGGTGCAGGT CCACCCACCT CCCCACTTTC 3180
CCAAACCTTC CTCCTTTTCC ATTTAGAGAC TGTCCCTGAG TCCCAATTTC CATGTCACTC 3240
TGGAAGTGTG AAAGTGATCT TTATTCCCCA TACCTTCTCT ATTTTTAAGC AACACAGTTA 3300
ACTCACTCTG TACTGGTTCA GCTGGTGAGG ATCCATATTT TTATTTTCCC CTAAGAGTTC 3360
CCAGCCTCTA AACAATACAT TCTGACAAAA CAGGTTAATT TAAGTTGCTA ATTATTTACA 3420
TTATTAAAAC ATTATTACAT TTGCACATGT AATAATGTCT ACATACTGAT TACACACACA 3480
CACACACACA CACACAAACC TAAACTGGCA TAATCCCTGG TTAATATGCT AATAATAAAA 3540
TTGATGATTA CTAAGTTGAA AAAGTTAATT AGCTGTCTTC TGTTTTTGTA TGTGGGGCCT 3600
AATCCTCCCT GTGATCTTGG GCCCAACACA TTTCTCAAAG GCCACACCAG TCAGAAGGTA 3660
GATTTTCCAG TTGGAAGGTA TTGAGAGCAT TGCAGGGGTA AACCCAGTAC CAGTCCACCC 3720
TGGGAGGACA TATGTCATTA TACTGAGAAT CAAGTATCAG GAAGTATAGT ATCATCATCA 3780
TCATCATCAT CAATCAATGA CTAACTGTGA GTTTATTTCC TTTTGTTTTT ATTTTTTAAT 3840
TTTAATTTTA TTTTTTTCTG AGACGGGGTC TCAGTCTGTT GCCCAGGCTG GAGTGCAGTG 3900
GCGTGATGTT GATTTACTGC AACCTCTGCC TCCTGGGTTC AAGCAATTAT CCTGCCTCAG 3960
CCTCCCGAGT AGCTGGGACT ACAGGCGTGC ACCACCATGG CAGACTAATT TTTTATATTT 4020
TTAGTACAGA CAGGATTTCA CCACATTGGC CAGGCTGGTC TTGAACTCCA ACTCCTGACC 4080
TCAAGTGATC TGCCCGCCTC AGCCTCCCAA AGTGCTGGAA TTACAGGCAT GAGCCACCGC 4140
ACCCAGCCCA TTTCCTTTTG TTTTTAATCA ATTTAGAACT GAATTCTCAA GCTGCTGTTT 4200
GTTTTGATTC TAGGCATATT TTGATATTCC AGTTAGTACC CAATTCAGTT TATATATGTA 4260
TAAAATTACA CACCCTGCAT CAAAAACATC TTTACATATT TTTATACTTA AACCCAGTTC 4320
AAATTGATTT AAGGCTTAGG AAAATAAGTT AGGTTTAGTT CAGTATGTGG TTTAGAAAAT 4380
GTGTACACTT TATTCTGGCT TCCAACTAAA ACTGTGGTGT GTTTCTTGCC TCTGAATTGG 4440
ACAGATTTCT ATGTTTGGCC TGTATTGTGG CAATGGTGTA TTATTTTGTT CTTGTCAGTT 4500
GCATTCATCA TTATTTTAAA AAGATTCCAG AAAGCCTGGT GTTACAGTTA GCCCACCTTG 4560
ACCCTAAATG CTGCACTACT GCATTTTGAC CAAGCATTGG GATCATAAAA 4610
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