Tag | Content |
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EnhancerAtlas ID | HS034-00223 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr1:8130210-8131350 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxq1 | MA0040.1 | chr1:8130327-8130338 | TATTGTTTATA | + | 6.32 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_28462 | chr1:8130335-8131180 | Fetal_Intestine | SE_29143 | chr1:8130309-8131077 | Fetal_Intestine_Large | SE_33765 | chr1:8129803-8132279 | HCC1954 | SE_34231 | chr1:8130145-8139927 | HCT-116 | SE_36051 | chr1:8130304-8131465 | HMEC | SE_36931 | chr1:8130052-8131152 | HSMMtube | SE_47106 | chr1:8129470-8148808 | Panc1 | SE_51696 | chr1:8130323-8131147 | Skeletal_Muscle_Myoblast | SE_52775 | chr1:8130251-8130925 | Small_Intestine | SE_57523 | chr1:8130534-8130885 | VACO_503 | SE_63484 | chr1:8130309-8131147 | HSMM | SE_65162 | chr1:8130100-8131523 | NHEK |
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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 |
GH01I008069 | chr1 | 8129686 | 8132169 |
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Enhancer Sequence | TCTTTTTATG TATAATTTTT TTTTTTTTGA GACAGAGTCT TTCTCTGTCA CTCAGGCTGG 60 AGTGCAGTGG TGCAATCATG GCTCACTGCA GCCTCAAACT CCTGGGCTCA AGCTATGTAT 120 TGTTTATATA TACATACAGG TGAAAAAATG TGTGTGTGTG TGTACACACA CATAGATTAT 180 TTGAATTTAA AATATATGGA TAAACACATA TATACATGTT TTAAATTCAG AAAACCTTGA 240 TGGTGTTTGA AGGTAGACTC CTGAGGACTT GAGGGAAGGA AGGGGTTAAA CAAGGCACTG 300 GGCAAGCGTG GGGCAGACTT CTCGTCAGGA AATCTGGTAT TTCAGGTTGG ACTGGACTTT 360 GGAGATGGCT GCTCCTTTGT TCAAGTGAAA AAATGCTTTA GATCTGGCTG CGCTCTCAGA 420 TGTGACTTGT ACAAAATGAA TTCTAGACTT TTCTCGCATC AAGAAAGTGA AGTGGGGCCT 480 TCCGGTAACT TGAACAGACT TTACCCCGGG AATCCCAGAC AGCAGCATCT CCGATTCCCT 540 AAAGTGTGCA CAATTACAGC TGTGGCAACC GACCCTAGGA AGGCTCAGCA CCACAGCGAA 600 CCCGAGAATA TTGGGAATAA ACTTGGAAAT GTGGAGATAG GTTCAACAAA CCTTTGGGTG 660 TTCAGCTGTT TTTTTACACA AAGCCGTTTA TTTAGTATTA GATTACTGTG AGATTTCACA 720 TTTTCTGTGA GAGGAATTCT TAAGTAACAG TGATAGTGAA GTTGCCAGGT TTACCTCCAC 780 ATGATTTTGT TTTCTTAGTC TCTATATTTT GGGATTCATT TATTTATATT TCTCCAATGA 840 CCAGCACCTA TCCTGTAGAT TACTTCTTGC AGAAACTTTT TTTTTTTAGT TGCTTCATTT 900 AACCTGTGAC TAATTGGTTA AATAAAAACA ACATGTACTC CTCGTATTTA CAAGTACATT 960 TCGTTCTGGG CCAGATAAAA AGGAGTAAAT TACACTGTTC ATTCCTGTCG TTTTTTATCC 1020 CTCCCTTTCC TTCAAAATTA TAAACAAAAT TTACATTAGA AAGTTCTTAA TTGCTTAAAT 1080 AGTGTTCCTA GTGTTTATTT AGGTTTATTT TACTCAATTT ATTTTTTGAG ATGGAGCCCC 1140
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