Tag | Content |
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EnhancerAtlas ID | HS105-40942 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr19:49850620-49851950 |
Target genes | Number: 38 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr19:49851325-49851344 | TTCCTCCATCTGCTGGCCA | - | 6.57 | PBX1 | MA0070.1 | chr19:49851114-49851126 | TTTGATTGATGT | - | 6.74 | TFAP2C | MA0524.2 | chr19:49850995-49851007 | AGCCCCAGGGCA | + | 6.11 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_58754 | chr19:49827549-49861083 | Ly1 | SE_60095 | chr19:49827676-49860875 | Ly4 | SE_61272 | chr19:49828268-49861182 | HBL1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 49851722 | 49851816 | chr19 | 49851050 | 49851462 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I049347 | chr19 | 49851201 | 49851370 |
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Enhancer Sequence | CTGAGGAGGG TTGGCCGTGG GTGAGAAGTC GGAGGTGAGC TGGATCTCCA GCCTGTGCTG 60 CCTGAGCCCA CCAAATGCCG TCACCATCCC CACAGCTCTG GCCAGCTGTT CCACACAGTC 120 CACCCAGCAC TGGGCCTGAC TGCCACCCAT CGTCCCCACT CCTGCTTCTG CACCCAGTCC 180 CCTGCAGCCC TGCAGTCCTA CAGTCCCCAA CTCCCTGCCA CAACTCCCCC AACTCCATCC 240 TCACTGCCTC AGCCTCACCT CAGGCCTCCC ACCCTCACCC CAGCCTCCAA CCTCGCCTCT 300 CCAGTTCATC CCTCATGTGG CTCCAGACCT GCCCCTGACC CTCCCCTGGT CATGGCCCTC 360 CCATAGCTCC CCAGCAGCCC CAGGGCAAAG CTCACACCCC CTAGGCCTGG TCCTATATAG 420 AACAGGTGCT CATAAATGGT CAATGGATGG AAGAGTGAAT GAATGGGAAT CCACAGAGGT 480 CTTGTGGTTG ATGTTTTGAT TGATGTTTAT ATGGTGTGGC AGAGACTGCT ACGTGTTCAC 540 AAATCCTGGT TCCTTTACAC AGTGTGAAAC TACATTTCCC AGGCCGCTTT GCAGTTAGGT 600 GTGACCACAT GACTAAGTTC TGGCCAATGG GATGTGACCA GGCCTGAGAG TCGACACATC 660 CAAGTCAGAT TCCTAAAACC TCCTGCACAA TCTTGACTCT CTCCCTTCCT CCATCTGCTG 720 GCCAGATGCA GAGACTCCAT CAGCAGATTC TGAAGCCTTA GAAAATGGCA GAGCCACAAA 780 ATGGAAGGAG CCTGGATCCC CAAATCACTT GAGTCCAAGG CTCCTGCTGA ACCTACATTG 840 AAATGTTACA TGCAACTTAT CTGGCATTCA GTCCCTAAGA GTTAGGAGCT GTTTCTTCTA 900 ACAGTCGGCC CACTCCATCC TAGCCCAGGA GAAGCTCAAG CACAGAAATA AAATCTTTTC 960 CAAGTTCCTA GTATGCATCA CAAAGCCTAG TGAACAGTAG AAACTCAAAC ACGTTTGATA 1020 AATGAATGAA TGATGTCCTG GGGAGCTTTT CTGACCTTCC CAACTTGTCA CCCTATGACC 1080 TTCCAGTTCC TTTATGCTAG TAGTTCTCAA AGTACGGTCC CCAGACCAGC TGCATCAACG 1140 CACCTGGTAG CTTATTAGAA ATGCAAATTC TCAAGCCCCA CATCACATCT AGCAAATCAG 1200 AAAGCAATCT CTGTTTTAAG AAGCCCTTCA GATGATTCTG ATACATGCTA AAGTTTTAAA 1260 ACCATGACTT TATACATTCC CTTCCTGTCA CCCTCTATAT TTCAAAATCC CTCAGCGACT 1320 GTACCAAAAT 1330
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