Tag | Content |
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EnhancerAtlas ID | HS145-20900 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr5:76101650-76102450 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr5:76102261-76102282 | TTTCTCTTCCCATCCTCCTCT | - | 6.54 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_02376 | chr5:76099767-76104689 | Astrocytes | SE_28159 | chr5:76101062-76102655 | Fetal_Intestine | SE_28864 | chr5:76099647-76103667 | Fetal_Intestine_Large | SE_34546 | chr5:76101274-76103861 | HCT-116 | SE_36755 | chr5:76101847-76102613 | HMEC | SE_38350 | chr5:76100878-76104589 | HUVEC | SE_46266 | chr5:76099642-76104431 | Osteoblasts |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH05I076804 | chr5 | 76099832 | 76105605 |
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Enhancer Sequence | AAAACAACAA AAGCTTTTAA AGATTTAAAG TTAGTTTTAT TCAGAAGTCT TACTGAGGGC 60 TATAGACCAA GGCCTGTAGC CCAGGAGCAG TTCTATGAGA CTGCTGGGGC ACAGTATCTC 120 AGCCCATGGC CCATATACAG GCGGTGGGGG TTCAATATGT TCAAAGTCAC ATGAGACTTG 180 CTCAGAAGTT GCATTCAAGC AGAATCACAT TGACGTTTCG GTGTAAGAGC ACAACTGGTT 240 ATAGATTACA GAGGCATCAT CACTGACCTT GTCAGAGGTT ATCTTATGTG TAGGCAAAGA 300 CAAACACTGC GGTCATTTAT CTTTTAAGGA ATATAGTGAC TCAGGCAAGA GATGTCCTGT 360 TTTGTCTTCT AAGCATCTTT CCAGAGAGCT GTGTGTAGAC ACAGAGTCAG GAGCTTCGAG 420 AAATTAAGCA AGCAGAAATG AGCAAACATG ACTTCTTAAC ATTTGCTACT TTGTCTCATA 480 TGACTCACCA AGGAAGAAGG GATTTTAGCA TCTGACAAGC CAGCTGTAGC TTTGAAGACT 540 GTTTAGGGAG CCTGCTGGGC ACTGAGTAAT AAGCAATTTG CATCGCACTT CTGTAGTATC 600 TTGCATCTTG GTTTCTCTTC CCATCCTCCT CTTCATAGCT CCCTCCTCTT TTGGCTCATC 660 CACCGCTAAC TTAGTCTTTG ATGCTTTTAC TTTGACCCCC AGGACTTTCC TGTTGGAGTG 720 AGCAGGTCGG TTTTCTTTGA GCTGTGCAGC AGCAGTCTCC TTGGCTAAAC TCAATCCAGC 780 ACAGGACCAC TCCCAAGAAA 800
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