Tag | Content |
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EnhancerAtlas ID | HS102-00142 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr1:9204720-9207280 |
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) |
CREB1 | MA0018.3 | chr1:9205463-9205475 | AGTGACGTCACC | + | 6.22 | CREB1 | MA0018.3 | chr1:9205463-9205475 | AGTGACGTCACC | - | 6.22 | Gfi1b | MA0483.1 | chr1:9205720-9205731 | AGCTGTGATTT | - | 6.14 | SOX10 | MA0442.2 | chr1:9206074-9206085 | TGCTTTGTTTT | - | 6.02 | TEAD1 | MA0090.2 | chr1:9207052-9207062 | CACATTCCAT | + | 6.02 | ZNF263 | MA0528.1 | chr1:9206343-9206364 | TTCTCCTTCTCCTCCTCCTCC | - | 10.09 | ZNF263 | MA0528.1 | chr1:9206364-9206385 | TCCTCCTCCTCGTCCTCCTCC | - | 10.26 | ZNF263 | MA0528.1 | chr1:9206346-9206367 | TCCTTCTCCTCCTCCTCCTCC | - | 10.48 | ZNF263 | MA0528.1 | chr1:9206349-9206370 | TTCTCCTCCTCCTCCTCCTCC | - | 10.92 | ZNF263 | MA0528.1 | chr1:9206352-9206373 | TCCTCCTCCTCCTCCTCCTCC | - | 12.34 | ZNF263 | MA0528.1 | chr1:9206399-9206420 | TCCTCCTCCTCCTCTTCCTGC | - | 6.06 | ZNF263 | MA0528.1 | chr1:9206370-9206391 | TCCTCGTCCTCCTCCTCCCCC | - | 6.41 | ZNF263 | MA0528.1 | chr1:9206387-9206408 | CCCCCGCCCCCTTCCTCCTCC | - | 6.44 | ZNF263 | MA0528.1 | chr1:9206384-9206405 | CTCCCCCCGCCCCCTTCCTCC | - | 6.54 | ZNF263 | MA0528.1 | chr1:9206408-9206429 | TCCTCTTCCTGCTCCTTCCCC | - | 6.5 | ZNF263 | MA0528.1 | chr1:9206358-9206379 | TCCTCCTCCTCCTCCTCGTCC | - | 6.92 | ZNF263 | MA0528.1 | chr1:9206340-9206361 | CATTTCTCCTTCTCCTCCTCC | - | 7.16 | ZNF263 | MA0528.1 | chr1:9206390-9206411 | CCGCCCCCTTCCTCCTCCTCC | - | 7.36 | ZNF263 | MA0528.1 | chr1:9206396-9206417 | CCTTCCTCCTCCTCCTCTTCC | - | 8.17 | ZNF263 | MA0528.1 | chr1:9206405-9206426 | TCCTCCTCTTCCTGCTCCTTC | - | 8.45 | ZNF263 | MA0528.1 | chr1:9206355-9206376 | TCCTCCTCCTCCTCCTCCTCG | - | 8.54 | ZNF263 | MA0528.1 | chr1:9206393-9206414 | CCCCCTTCCTCCTCCTCCTCT | - | 8.97 | ZNF263 | MA0528.1 | chr1:9206367-9206388 | TCCTCCTCGTCCTCCTCCTCC | - | 9.24 | ZNF263 | MA0528.1 | chr1:9206361-9206382 | TCCTCCTCCTCCTCGTCCTCC | - | 9.29 | ZNF263 | MA0528.1 | chr1:9206402-9206423 | TCCTCCTCCTCTTCCTGCTCC | - | 9.54 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_01288 | chr1:9204907-9205661 | Adrenal_Gland | SE_45801 | chr1:9204852-9206131 | Osteoblasts |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I009145 | chr1 | 9205096 | 9205905 |
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Enhancer Sequence | ACAGCATCTC CAAGCCGAGC AGAGAGTCCT GGCGGGGCCG CGCGCGGTGG CTCATACCTG 60 TAATCCCAGC ACTTTGGGAG GCCAAGGCAG GTGGATTACT TAAGGTCAGG AGTTTGAGAC 120 CAGCCTGGCC AACATGGTGA AACCTCATCT CTACTAAAAA TACAAAAATT AGCCTGGTGT 180 GATGGGCCAC ACTTGTGTTC CCAGCTACTT GGGAGGCTGA GGCAGGAGAA TCACTTGAAC 240 CTGGGAGGCG GAGGTTGCAA ATGGATACAA CTCACTAAAC CAGTAAGATC CCTTCCTACA 300 TCCTGAGGAA CTACCTGTAG GAGTTTCTGA CGGGGACCAG AGGCAGCCTG TACAGGGGGC 360 CTGGGGCTCT CTATGTGTGT GTGTCCCGGG GCAGCCCTGG GTTTGGTGAG AGGGAGGATT 420 CTGATCTCAC TCAGCCCTAC TCACTCCGGC CCTCTTGGGA AGTGGGTACC AAGCCCTGAT 480 CCCACCCGGG CTGGTGCAGG ATGGTGGCAT CCCCGTGGCC TGCAGCCGAG CCCTGTGGAA 540 GGCCGCTGGG CAGAGACAGC TCCTCCGTTC ACAGGACCCT CATCCAAAAA CCCTCACATA 600 TTTCAACATA GCCGCACCCC GAACGTGGAC CCCTCAGGCA CCGGGCCCTG TGTGGCCATC 660 CAGGCTGCAC ACCCATGAAG CCAGCTCTGC TGCTGGGGGA CAGCAGAGAG AGGAACAGGC 720 AGGCCGAAAG GTGTCCAGGG CACAGTGACG TCACCAGGAG CCACTGAGTC ATCAGGAGGG 780 CCTTTCATCA GTCGGCTGCC TGGTCTGATC TGAGCGAGGT GGAAGCTTCC AAGGCCAGAC 840 ACGGGGAGAC TCTGTGAGGC TCCCACATTG TTGATCATTT CTTCTCATCT CTCCTCTCCT 900 GACCAGATTG CTCTCTAACC AGATTCATTT CAGGAGTAAG TGACTGCCGG CCAAGAAAGA 960 CAACCCCCTC AAGGTTACTA ATTTAAAGAC AGATGGGATC AGCTGTGATT TCAGTCGCAG 1020 TTATGAAAAT TAGAGCCAGG TGTGGTGGCT CATACCTGTA ATCTCAGCAC TTTGGGAGGC 1080 TGAGGTGGGA GAACTGCTTG AGTCGAGGAG TTAGAGACCA GCCTGGGCAA CATAATGAGA 1140 CCCCTTGTCT TTAGAAAAAA TGTAAACATT TGCCAAGTGT GATGGCGTAC ACCTGTAGTC 1200 CCAGCTACTT AGGAGGCTGA GGTGGGAGGC TCGCCTGAGC CCAAGAGGTC AAGGTTGCAG 1260 TGAGCCATGA TCGCACACTG CACTTCAGCC TGGGCAACAG AGCAAGACCC TGTCTCAGGA 1320 AAAAAAAAAA GGAAAAGAAA ATTAGACTAA GACATGCTTT GTTTTGCAAT GGTGCAGCAT 1380 CAAGGGGTCC TGGCAGGGAA GAGGTGGCAC CAGCCTGCAC CACTGCTGCA GAAATACTCG 1440 GGAGTACACA AAGCACTTCT CGGCTGGAGT CCAGAGGCCT TCATATTTGG TAGTTTACTC 1500 TGATGTTTTC AGTTCCAACA GAGGAAGAGG AAGGGGCTGG TCCACAGTGG CCTCAGGTAA 1560 TGCTCAGCCT TGGGGGATGA TGAACACAAT GAGGGGCACT TGGCGTGAAG AGTGAGAGTC 1620 CATTTCTCCT TCTCCTCCTC CTCCTCCTCC TCCTCGTCCT CCTCCTCCCC CCGCCCCCTT 1680 CCTCCTCCTC CTCTTCCTGC TCCTTCCCCC TACCCTCCCC ACACGGGAGG TGTATCAGGT 1740 AGTGAGTTTC AGCCCGGCAC GGTGGCTCAT GCCTGTAATC CCAGCATTTT GGAAGGCTGA 1800 GCCAGGCGGT TCACTTGAGG CCAGGAGTTC GAGACAAGCC TGGGCAACAT GGTGAAACCC 1860 TGTCTCTACT ATTAACAAAG TTACAAAAAT TAGGCATGGT GGGGTGTGAC TGTAGTCCCA 1920 GCTACTCGGG AGGCTGAGGC AGGAGAATTG CTTGAACCCA GAAGGCGAAG ATTACAGTGA 1980 GTCTAGATCG TGCCACTCTA CTCCAGGCTG GGCGACGGAG ACTCTGTCTC AAAAAAATAT 2040 TATTTCTTGA GGTCAGGAAT TCAAGATCAG CCTGCCCAAC AAGGTGAAAC CCGGTCTCTA 2100 CTAAAAACAC AAAAAAATTA GCTGGACGTG GTGGCGCACA TCTGCAATCC CAGCTACTTA 2160 GGAGGCTGAG GCATGAGAAT CGCTTGAATC TGGGAGGCAG AGGTTGCAGT GAGCCGAGAT 2220 CACGCCACTG CACTCCAGCG AAACTCTATC TCGAACATAC ATACATACAG CAAGCTCTCA 2280 ATGGGGCCAG TGAGCTGTGA GCATGTTTCC TCTGCACGCT AAGCTCTTGA CTCACATTCC 2340 ATCAGGAAGT TGGGGTCATC TTGACCAGGG AAGGGCAGGC ATCTTGGTGG GGGGCCCCTG 2400 GACTGTACCT GGTAGTGCTG CTAGCAGAGG AATGGAAGCT GGGCAGCAAA AACCCCTGAT 2460 GCCCACTAGT CCTGAGCATC CCTGGAAGCA TCCTGCCAAG TGCAAGGCCC AGGGTAAGTG 2520 CTGAATTAAT ACTTGCATTT TGCCTGGATC CTCACCCCAC 2560
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