Tag | Content |
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EnhancerAtlas ID | HS051-11394 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr17:17570140-17574170 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr17:17573034-17573052 | CCCTCCATCCTCCCTTCC | - | 6.98 | KLF4 | MA0039.3 | chr17:17571495-17571506 | CCACACCCTGC | + | 6.62 | Klf1 | MA0493.1 | chr17:17571493-17571504 | GGCCACACCCT | + | 6.32 | PHOX2A | MA0713.1 | chr17:17574155-17574166 | TAATTAGATTA | - | 6.32 | PROP1 | MA0715.1 | chr17:17574155-17574166 | TAATTAGATTA | - | 6.14 | Phox2b | MA0681.1 | chr17:17574155-17574166 | TAATTAGATTA | - | 6.32 | RFX2 | MA0600.2 | chr17:17572966-17572982 | TGTTACTATGGTGACC | - | 6.01 | RFX2 | MA0600.2 | chr17:17572966-17572982 | TGTTACTATGGTGACC | + | 6.11 | RFX5 | MA0510.2 | chr17:17572966-17572982 | TGTTACTATGGTGACC | + | 6.08 | RREB1 | MA0073.1 | chr17:17572014-17572034 | CCCCCTCCCACCCCCTCCCG | + | 6.5 | SCRT1 | MA0743.1 | chr17:17571013-17571028 | CAGCAACAGGTGGGG | + | 6.19 | SCRT1 | MA0743.1 | chr17:17570724-17570739 | CAGCAACAGGTGGCA | + | 6.6 | SCRT2 | MA0744.1 | chr17:17570724-17570737 | CAGCAACAGGTGG | + | 6.29 | SCRT2 | MA0744.1 | chr17:17571013-17571026 | CAGCAACAGGTGG | + | 6.29 | SNAI2 | MA0745.2 | chr17:17573719-17573729 | AACAGGTGCA | + | 6.02 | ZEB1 | MA0103.3 | chr17:17573322-17573333 | CCCACCTGCCC | + | 6.14 | ZNF263 | MA0528.1 | chr17:17573018-17573039 | ATCCCCACTCCCTCCTCCCTC | - | 6.07 | ZNF263 | MA0528.1 | chr17:17572575-17572596 | TCCTCTCTCCCTCCCGCCTCT | - | 6.15 | ZNF263 | MA0528.1 | chr17:17573087-17573108 | CCCTTCCCCACTCCCTGCCCC | - | 6.18 | ZNF263 | MA0528.1 | chr17:17573068-17573089 | TCCCTCCCCATCCCATCCTCC | - | 6.37 | ZNF263 | MA0528.1 | chr17:17573015-17573036 | CCCATCCCCACTCCCTCCTCC | - | 6.82 | ZNF263 | MA0528.1 | chr17:17573039-17573060 | CATCCTCCCTTCCCCTCCCCC | - | 6 | ZNF263 | MA0528.1 | chr17:17573026-17573047 | TCCCTCCTCCCTCCATCCTCC | - | 7.23 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_23508 | chr17:17571510-17572016 | Colon_Crypt_1 | SE_23959 | chr17:17571586-17572057 | Colon_Crypt_2 | SE_23959 | chr17:17572085-17572609 | Colon_Crypt_2 | SE_24961 | chr17:17571558-17571998 | Colon_Crypt_3 | SE_24961 | chr17:17572050-17572902 | Colon_Crypt_3 | SE_33725 | chr17:17568659-17574731 | H2171 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 17572079 | 17572678 | chr17 | 17573532 | 17573683 |
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| Number: 3 | ID | Chromosome | Start | End |
GH17I017668 | chr17 | 17571511 | 17572057 | GH17I017669 | chr17 | 17572161 | 17572310 | GH17I017671 | chr17 | 17573935 | 17574232 |
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Enhancer Sequence | AGCCCAGGAT CATCTCCTTA TCTCAAGACC TTTAACTTTG CACATCTGCA GGAGCCCATT 60 TTTTGGCTGT AAAGGGGACA CCCACACGTT CCAGGGATGA GGACCTGGAT ATCTTTAGGG 120 GCCATTTTTC AGCCTACCAT CATGAGCCGC AGACACTCCG TGGCCAGCTC CCAAACTTAG 180 CTCTGGCTGT GGGGCCGGGT ACAGTGACAG ACCTGAGACC CCATCAGCGC TGACACCATA 240 GGCCCCAAGA GCCTGTGACC ATGGCTGGTG AGAGCTCCCC AGAACAGTGG GGCTCTCAGA 300 GAAGTAGAGT GAGGAGCACA GAGAGACGGA TGGGTAGGTC CTGGGAGCAG GAAGGTATGA 360 ATTCAGGGGA GGCACACCGT GGCCTCCAAG CTGGGCCTCC ACAGTGTCTC ACTTCATCTT 420 CCCACAGCCC TTGACAGATT AGGAAACCAA GGCTCACAGA AGCAACAGCT AAGTCCTCTG 480 TGCAGCTTAC CTCTGAACGG CCCCACAGAG AAGCTGTTAG CAGCTCCAAG TTACAGGGGG 540 AGGAAGTGCC TGCTCAGAGG TGATGTGACT TGCCCAAGGT CACACAGCAA CAGGTGGCAG 600 GGCAGAAGCA TGAGCCCTCT GGCTGACTCA AGCACCCACC TTCTTGGTGC CTCACCAGGT 660 TCCCAGAAGC CAGAGGGTGA GCTGGTTTTG GAGAATGACC AGGATTTGGG GAAATGGAGA 720 AGGAGGGTAG ATGAACTTTG AGAGCTGAGT GGATCAATGG GATTTTTTTC TGGCTTTGGA 780 GGGAGGTGAC CTCAGCGTGG GGGTCAGTGT CTCTGCTATT GGGCAGGTTC CTCCTCTCAG 840 GGGCCCCAGA ACAGACTCCA ACAACGTCCA TCCCAGCAAC AGGTGGGGGT CTTGGGAGGG 900 TTATGTCTAA AGGGCTGTGT TCACCCCACA GATGACTCTC AGGGGCCTGC CATGGCCCCT 960 CCCTCCTTGG TTTTTTCTCC CTTTTGTCTG CTGCCCCCAT CCCACAGGCC CTGGAGGGCA 1020 GCAGGAAGGA GAAGGGCAGG GGTTGTGGCA TGGCTGAGTG CACCCTCATT TCTAGGGACT 1080 CAGGAGAGCA GAAAGAGCTG AGTGCCCCCC AGGAGCAAGC CAGGAAGGGG CCATTCTTGC 1140 CTCCAGCGGT GGCTGGGAGC TGGCCCCATC AGGAATGGGG TAAGGCTCCA ACCAGCAGCC 1200 CTGAGACCCC AGCCTGGCCC TCTAGGGCTG CACACAGAGT TGCACACACC CCACCCACGT 1260 GTGTGGACAG ATGCACACCC CTCCCTCCTT ACACCTGGGC CTCTAACAAC AGTTAGATGC 1320 CACAGAGGGC CTGGGCACGC CATCTGTTGT TCAGGCCACA CCCTGCTCTT GCTCAGGTGG 1380 AAAACTCTGG AGTGTCCTGG GCTCCTCTCC TCACCCCACG TCAGAAATTC TTGTCTATTC 1440 TACCTTCAAG GTATATTTGG AATTGGAATC TTTTCATTGC CCACAGCCCC ACCCTGGCCA 1500 GGGCCCCCTG GATTCCCAGG CCTCCTGCTC CTGCCCTGGC CCCTCTCAGC AGCCAGGGTG 1560 CACTGTGAGG ACCTAGGGGA GATCCCAGCT CTCCCTGAAG GACCCCGTCA CTCAGGGTCT 1620 GAGCCAGAGG CCCCACTGTA CACTGTGGCC ACCCAAGCTG GTCCTGACCC TCTCTGTCCT 1680 TGCCTCCTGC TCTCTGCCCC CATGCATTGC TCTTCAGCCC CACAGGCCTC CCCACTGCTC 1740 CCGGCACACT CCTGCCTCAG GACCTTTACA CCTGCTGTCT CCTCTTCCCA GCTCCCCACA 1800 CATCTGTCCC CTGCCTCCCT CAGGTCTCTA GAGGCTCTAA GACCACCTTC TCTCACCTAA 1860 CTAACAAGCT GCTTCCCCCT CCCACCCCCT CCCGCACCCC CTGGGACACT CATCATCCAT 1920 AGCTCCTATA TTTACCTTTC TATTTTGTCT GTCTCTCTCC TGCCCCAGAT ACCCACTAGA 1980 ATGTTGGCTC CATGAGGACA TGGATTTGTG TCTGCTTCAG TCACTGTTGC ACCCCTACCC 2040 AGCCCAGCAT CCGGGGCATT GCAGGCTCTA ACACCTGTGG AGGGAAAGAG TGCAGACAGA 2100 GACAGGCAGG GGCAGGTGAC CTGTACACAC TCAAGGCCTA GCGGGGCACT GGCACAGCTG 2160 CACATGCCCA CACCTGCGCA CACACACGCA CACGCGCGCG CGCACACACA CACACACGGG 2220 CCCTGAGCTG AATGCCCTTG GCTCAGTGGG GCCTTGGACG ACAGTCTGGC CCTGGCTCTT 2280 GGGCAGCTGG AGTCTTTGTC CTCACCCAAG ACTGCCAGCC CACCCCAGCT GTGGCTGCTG 2340 ATGCCCCAGA TGGGCCTGCA CTTCTGAAGA GAAAGGACCA GTTTCCTGCA GCCAAACCTC 2400 CAGTGCAGAC CACAGAGCAG CCACGGCATC TGAGCTCCTC TCTCCCTCCC GCCTCTGCAT 2460 CCCTGACTCA TCCCCCACCC CAGGGAGGCA GCCTAGGCCC AACTGCCCCA CTGAGCAGAA 2520 GGGAAGGCTG AGGCAGGAGG CTGAGCCAGC CAGCTGCCCC CGTTAAAGGA GAAGCAGATA 2580 GACGTGGCTT CCAGCCCAGC CCCTCCCTGG CTCAAGCGGT CACCTCCCAA ACAGTCTGAC 2640 CGCAGTCTGT GGGGGCTCCC TGGGCACCCT TGAGCCATGC GTGTGCAGCC AGTATGCACA 2700 CTCCCGCCAG CCGGCCCCTC CAGCCCAGCT TATCACTGAT GACTTTCCCA ACAGAGATCG 2760 ATAGAAAACC TTTTATCTCC TTCCCCGTGG TGGCTCAGAC TCAGGCCTCA GAGCAGAGCT 2820 GGCTCCTGTT ACTATGGTGA CCCTCAAGGA CCTCACTGAC TCCCTCCCAT TCACCCCCAT 2880 CCCCACTCCC TCCTCCCTCC ATCCTCCCTT CCCCTCCCCC ACTCCCACTC CCTCCCCATC 2940 CCATCCTCCC TTCCCCACTC CCTGCCCCAG CCCCTCTCCT ACTCCCTCCC CACCCCCATC 3000 CCACAGCCTG GGATCAATGC TGGTTCCCTA CAGGGCCTGC ACACCTCCCG GCTGCTCATG 3060 GCTGACAGGG AGGGGCCTGG GGGGCTCCTT GCACCCACCC AAGCCCCATC TGCTCCTGGT 3120 CTCGACCTTG CCAGTCCCCC ACTTTCATGC CAAACTACAG CTCCAGTGCC CGATTGAGGC 3180 CTCCCACCTG CCCACACCGT CCTCAGCATT CTGTAACTGC TCACTTATAT CAATGAGTTG 3240 TTTCCCCCTC CATACAGACA GATGGCACCC CTCCATACAG GGCTGCTGGG AGCTGTGAGC 3300 ATTACATAAG CACAAACCTA TGTTGAGTTT GGCCTGTGGC TGATGCTCAA GATATACTAG 3360 CCATTGTTAA TAAGCCTCAA TTTGTGCATT TATTAAATAG GTATAAAAGG TATTATGGTT 3420 GTAAAGATTA AATGAGAGAC AGACACAAAT AGTTTAGCTC ACGGCCTGGC ACGTTCTAAA 3480 CACTACATCC ATGAAGGGAC ACACAGCCTC CCTTCTTCCT TAGCCTCCTT TCTTCCTTTG 3540 TTCTTTGAAG GTGTTTAGGT ATGGGGAGGA GGTGGGAGGA ACAGGTGCAT CCCCGCCCTC 3600 CATGGAGGCT CCATAGCCTT GGCCTGCAGC ATGCAGGCCA AGGAGAACAA TGCCCCATCA 3660 GGGTCCAAGT AACCTGTGCC CTCTCTCTGC CCACAAAGCT ATATTGGTTG TGCCTCACTT 3720 TGGCGGAGGC CAGATTTTCC TCCCATGTTA CCCTTGCCTT CCTGCCTGGA GGCCGGGGCT 3780 GCTCTCTTCC TTCTGCCTGG AATGCCTTGC CATACGGCCA GCCCCACAAT CAGGGAACCA 3840 TCTTCAAGGG AAGTGCTATG GCACCGAGAT CTGGAGCCAG ACCCCCCGGG TCCACATTGC 3900 AGCTGTGCCA CTGCTACCCT CTGAGGCAGC TGCACAGAGG CCTCCCAGGA CCCCACACCC 3960 TCATCCCCGG AGCCTACCAG TGCTCCCTCA GGTGGCAAAA GGGTCTTTGC AGACGTAATT 4020 AGATTACGGA 4030
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