| Tag | Content |
|---|
EnhancerAtlas ID | HS183-00009 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr1:1004300-1007120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr1:1004737-1004751 | GTGGGGGCGTGGCC | - | 6.39 | | KLF16 | MA0741.1 | chr1:1004739-1004750 | GGGGGCGTGGC | - | 6.62 | | KLF5 | MA0599.1 | chr1:1004502-1004512 | GCCCCGCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr1:1004521-1004531 | GCCCCGCCCC | + | 6.02 | | Klf1 | MA0493.1 | chr1:1005572-1005583 | TGGGTGTGGCC | - | 6.62 | | NKX2-5 | MA0063.2 | chr1:1006876-1006886 | CTCAAGTGGT | - | 6.02 | | NRF1 | MA0506.1 | chr1:1004721-1004732 | GCGCCTGCGCG | + | 6.14 | | RFX1 | MA0509.2 | chr1:1004774-1004790 | CGTCGCCATGGTGACC | + | 6.11 | | RFX1 | MA0509.2 | chr1:1004774-1004790 | CGTCGCCATGGTGACC | - | 6.12 | | RFX2 | MA0600.2 | chr1:1004774-1004790 | CGTCGCCATGGTGACC | + | 6.2 | | RFX2 | MA0600.2 | chr1:1004774-1004790 | CGTCGCCATGGTGACC | - | 6.2 | | SP1 | MA0079.4 | chr1:1004499-1004514 | CAAGCCCCGCCCCTC | + | 6.34 | | SP2 | MA0516.2 | chr1:1004498-1004515 | GCAAGCCCCGCCCCTCA | + | 6.23 | | SP3 | MA0746.2 | chr1:1004738-1004751 | TGGGGGCGTGGCC | - | 6.57 | | SP4 | MA0685.1 | chr1:1004499-1004516 | CAAGCCCCGCCCCTCAT | + | 6.24 | | SP8 | MA0747.1 | chr1:1004738-1004750 | TGGGGGCGTGGC | - | 6.11 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_24070 | chr1:1002554-1005867 | Colon_Crypt_2 | | SE_24817 | chr1:1002490-1006081 | Colon_Crypt_3 | | SE_27529 | chr1:1001798-1011077 | Esophagus | | SE_34539 | chr1:1004454-1006480 | HCT-116 | | SE_41944 | chr1:1001963-1005965 | LNCaP | | SE_58139 | chr1:1004236-1004768 | VACO_9m | | SE_58139 | chr1:1004812-1005267 | VACO_9m | | SE_65935 | chr1:1001682-1006445 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 1005293 | 1005547 | | chr1 | 1006044 | 1006328 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I001066 | chr1 | 1001837 | 1006486 |
|
Enhancer Sequence | TGGGGGCATC GGATGCACGG GCACCATCAT CGTGATTGAC ATCCTGGTGG ACGTCATCCG 60
CAGGCAGGGC GAGCCGCTCC ACTCTGGGTC CCCCCGCCCT GCCCTGCTAT AGCCCCACCC 120
CTCCGGGCGA CCCCACCCCT CCGGACGACC CCACCCCTCA GGACGACCCC ACCCCTCAGG 180
ACGACCCCAC CGCTACCGGC AAGCCCCGCC CCTCATCAGC AGCCCCGCCC CTGCCTGCCG 240
GCACCTTCCC CCCATCCGTA GCCCCTCCCC AAGCGCGCTT GTCCGCAGGG CTGGACTGCG 300
ACACCGACGT CCCGAAGACG ATCCAGCTGG TTTGGCGGCA GCACTGGGGA ATGGTGCAGA 360
CGGAGGCTCC GTACAAGTTC ACGTACCTGG CGCTGCAGCG GCACATCCGG GGCGAGTAAC 420
TGCGCCTGCG CGAGCAGGTG GGGGCGTGGC CCTGCGGGGC GTGGCCTGTG CGGGCGTCGC 480
CATGGTGACC GGCGGCCCCT CCCCCCAGCG CGAGCCGCCT CAGGAGCGCG AGAACCAAAA 540
CGTGGGCGCC GCCCCCCGCT AATCGGGTTG CAGCCCCCGG CTCCCCGGGC ATCCCCGGTG 600
TGAGTGGAGC GCCGGGGCCG GTCCGGAGTC CTCTGGGAGG GACTGGGACG TGCGGGGTGC 660
AGGGCTGAGC CGCTGCTCCG CGCGCAGAAC CCCGCAGCCC TGGGACGGCG AGGACGCGAA 720
CCTGCGGAGC CGCGGGTGTC TGAGGAGCCG CAGGGAACCC CCGGCCTAGC CGCGCCCGCG 780
TGTGGCCGGA GCTGCGGGCC GGGACTGTGT CCAGGACAGA GCCACAAGCT TGTCCCCAGC 840
TCAGGGAGGT CCAGGGGCGG CAGAGGGAGC GACAGGCTGC GAAGCCCACC GGTGACCACG 900
TGTGAACCCG CGTGCGCCCC CAGCTCGGCC ACTCCGTGCG GGTCTGCCCT CACCGCAGCT 960
CCGGCCTGCC GGCCCTGCCT GCTCCCGTGG TCTGGGATGT GGCCCCGGTG AGGACCCGGC 1020
CCCATCAGGC ACAGGGTGGA TGTCTGTGGA GTGAGGTGTG TGTGACATAT TCATGTGACC 1080
ACCCGTGCAG CGTCACGCGC CTGGCCCTGC CGATGACAAG GGTGTGGGCC TGCGTGGGCA 1140
TGACTGTGTG TGTGACACAG AGTGATGTTG CTGTGACCCG TGGCTGCACT CCCCACATCA 1200
CCGGCTTTCA CAGCCTTCCG GTAAAGTGCT GTGTTCTCCC TTCTGTGTCT TCGCTGGGAC 1260
CTGGGGCAAG GGTGGGTGTG GCCCCCACAG CTGGAGTCAG CTTCTGTGGG GCCTTCCCGA 1320
GCCCTCCCCA CCCTGGACCA GAGGCCCAGC TGGTTGGAGC AGGAAGTACC TGGGCTCTGG 1380
GGTCAGGGAT GGGAAGGCTG AGGAGGCCTG CGTGAGCTGG ACCTGGCCTG GGCCCTCCTG 1440
GCCGTGCCTG CCTGGTGGTG CAGGATTCCT GGGGCTGATG ACAGACGGGG TAGGGCTGGG 1500
GTTGGCGAGC CTCCTGCCGA TACCTCACGT AGCTGACCTC TGACTCTTCC CCAGCCAGGC 1560
TGGCCCTGGG AGTTGCCGGA GAGTCAGTGG ATCTGCAGGC TGCACGCTGG CTGTTACCTT 1620
TGCTTCTGGG TTCCCACAGG GGTCATGGTT CTGTGGTTCT CCAGTCAGGG ACCCTAGCAG 1680
GGCCATGGGG CGTGACTTCC TGGAGGTGTG GCCTAGTATG GCCACGGCAG AGGATGGGGG 1740
AAGAGAAAGG CCCCCTTTGT CAGCCCCCGG GCTCTGAACC AAGCTGAAGC CCTCCCCCTG 1800
GTCCAGCCTG CCCTGCCCCA AGTGTCCTGG GCCTCTCCCC ATCTCCCTGG GGAGCCTCAC 1860
ATTGCTGAGT CGCCAGCCAA CTCCAGAAAC CCCCAGCCTG TCTGCAGCCA GAGGGGCTGG 1920
GAGTTGGACC CCCTAGAACC TTGGGCCCAC CTGTCCCAGT GGCTGCTGGG AGTCTAATTC 1980
TGTCAGGGTA TCCTCTGGGT TGAGGCTGCA GCAGGGGCAC CCAGGGTGAG GCCCTCTTGC 2040
CAAAGATGGA TACAAATAAT TTATTTTAAA AGGTACAATT CACAAGGTTG GAGGGGTAGC 2100
TGGAAGTTTC TGTGGTTACC TTGCACTGGG GGGCTGCCCT GCCTCCACTC TCTCCCCACA 2160
GTCCGAGGGC AAGATGAGCA CCCCCACCCA ATGGCAGGAC CAGCCCTGCG GGGAAATGTC 2220
AGCATGAGTG GAAGCACGGC AAGGCCCCTT CCTTCTTGGC AAGGGGCTTC CCTGGCAGGC 2280
AGTTCACAGG GTGTGTGGGT GGGGGGGATG CTGACCAGCT GCTCTCCTGG ACCCTTCCTG 2340
TACGAGCCTG TTTTTTTTTG TTTTGTTTTG AGACAGGGTC TCCCTCTGTC GCCCAGGCTG 2400
GATGCAGTGG TGCAATCTTG GCTCACTGCC ACCTCCACCT CCCCGGTTCA AGCAGTTCTC 2460
CTGCCTCAGC CTCCCCAGTA GCTAAGAGGC ACCCACCACG ATGCCCGGTT AATTTTTGTA 2520
TTTTTAGTAG AGATGGGGTT TCACCATGTT GGCCAGGCTG GTGTCAAAAT CCCGACCTCA 2580
AGTGGTCTTT CTGCCTCAGC CCTCCAGAGT GCTGAGATGA CAGGCGTGAG CCACCGCGCC 2640
CGGTGAGACT GTGGTTCTTG GAGGCTTTGG GGATCCTCTT GTCCACCCCG TCAGGACCCA 2700
GCCTGGAGAA TGAGGGGTGG ACAAGCTAAA TGGAGCCTGG TCTTGGTGGG GCCCCGGTGG 2760
AGTCCTCAGA GATGCCAGGC TCCTTTCGCG TCCTCGGGGA CCGACTTCCA GTGGCTGCTG 2820
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