Tag | Content |
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EnhancerAtlas ID | HS048-22071 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:217522650-217524780 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Hnf4a | MA0114.3 | chr2:217523728-217523744 | GCTGGACTTTAACCCG | - | 6.18 | REL | MA0101.1 | chr2:217522768-217522778 | GGAAATCCCC | - | 6.02 | Spz1 | MA0111.1 | chr2:217523764-217523775 | GCTGCTACCCT | - | 6.02 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_01659 | chr2:217523496-217524848 | Aorta | SE_25399 | chr2:217523543-217525271 | DND41 | SE_26938 | chr2:217523482-217525014 | Esophagus | SE_27936 | chr2:217522389-217524879 | Fetal_Intestine | SE_29226 | chr2:217522134-217525039 | Fetal_Intestine_Large | SE_31800 | chr2:217523600-217524795 | Gastric | SE_58444 | chr2:217447610-217532079 | Ly1 | SE_68753 | chr2:217523550-217524959 | H9 |
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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 |
GH02I216657 | chr2 | 217522342 | 217524727 |
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Enhancer Sequence | ACAATTTTGG ATAAAAGTCT TTTAAAATGA TGAATAGGTA GAATTTTAAT TCCCTCCCCT 60 TTTTGATGTC CCAAGATCAT CGTCATCAAC GTAATTCTTG TTTTGGGCTG TAAGACATGG 120 AAATCCCCAG GGTTCATTGA GGGGCATTCA TTGTTTGCCA CACACAAAAT GTACCCGGAG 180 TTTGTATGTT TTGTTTTCTT AGTGTCCTCT TTCCTCTCTG CCATTTGATC CTTCTTGCTA 240 CTGTCCACAT GCATTCCTTC TTTGTCCCTT CAATTTTGTT GACTTTCTTC TGCGGTGGCC 300 TTGGAAACCA GACATCCAGA AGCCAGGCTT CCTGGAGCAG CACTGTTGTG AACTGTCTCG 360 AGGCTCCTCA CGAGATGATT CTCCCCTCAT CTTGAGTGGA AAGTGCCAAC ATTTGAACAT 420 GCTCAGCCGT GGTAACAGCT ATTAGGATGT TCAGAGCTTA TTTTCCTTGG TTTCCCTGTT 480 CTCGGTTGGG TTCCATGCTG CTGAAGTAGT AGATAACTGG GGCATTCGTC ATTGTCATCA 540 TCATCAGTGT AATAACCAGC AGCAACATGG ATATAGAATT TCTGTGCTCC AGGTCGTCTT 600 TTATTTATTT ATTTATTTAT TTATTTATTT ATTTATTTTT GAGGCAGTGT CTTGCTCTGT 660 CGCCCAGGCT GGAGTACAAT GGTGCGATCT CAGCTCACTG CAACCTCCAC CTCCTGGGTT 720 CAAGCAATTG TCCTGTGTCA CCCTTCTGAG TAGCTGGGAT TACAGGTGTG TGCCACCACA 780 CCCGGCTAAT TTTTTTGTAT TTTTAGCAGA GATGGGGTTT CACCATGTTG GCCAGGCTGG 840 TCTTGAATTC CTGACCTCAA GTGATCCACA TGCCTCAGCC TCCCAAAGTG CTGGGATTAT 900 AGGCATGAGC CACCACACCC GGCCTAAGTC ATCTTTTAAC TGCTTTTCTT TCGTCATACT 960 CTCAACAGCT CTATGAAGAA AGAACTGTTA TTATCCAGCA ACTTACAGTT AAGAAAGTAG 1020 AGGCACAGAG AGGGTCTGTG TGGGGAGAAC ACGTGCAGCT GATATAGAAA ATGGCAGAGC 1080 TGGACTTTAA CCCGGCTACA CCCCTTTAAC CAGAGCTGCT ACCCTGGGGA CGGCGTGCTG 1140 GCTTCTAAAG GAAGCTGCTG CATGGCAAGT GAAGAGTGAC TAGTTCTCAG GCTTGGAGGG 1200 AGGGGAAAGG ACAGGGACAG ACCCCCATCA AATGTTCCGT ATGCTGGGGC CTATGCTGGG 1260 CACGCCTTGA CAGCAGGTGC TGCTGGAGTG CCAGCACCCG GTGCTGTCCC TGGCATGGAA 1320 GAGGTGCCCC CTCCCTTAGT TGGTGAGTGA GTGAATACTC TTGTATAGAG TTACTCTAAG 1380 AATTATTCAT TTGTGTTCTA AGGGCTGTAA GTTTTTGAAG GTGCATTAAT GGGGAAGAAA 1440 AAATGTGCAA GATTGGTTGA AAAACACCCC TCTGCACCCA CCCAGATCTT GTTGGGACCT 1500 GCAGGAGAGC AGCTCTGGGT GGGAGGGTCT GGGGCTGTTT GCCGTGTCTC CAAGGGGTTG 1560 GGGCTGGGGC TCGGCGGTGT GAGGCCCTGC CCTTCTGGAG CTTGCTGGGG CTTGTCTCCT 1620 GGTTACAGCT CTGCCGTGCG ATTCAGATCC TCTCTGCCTC CTTTGGCTGG ACGTGCCTCA 1680 GCCAGAGTGA GACTGTGGCA GGCTGGAGCT GTTTTCAAGG CCTCCTTCAC CTAGGCTGTG 1740 CATACAAAAG GTTGAAGAAA GTATAAGGAG ACTTAATGGA CGCTTGTTGG ACAGACATCA 1800 CGAAGCTTCA TGCCCTGCAG TAAGCTGAAG CTATGAAGTC GAAGGAGTCA TAGTTCCTGT 1860 TCTTGGGGCT CTCAGTATAA TGGGGTTGGG GTGGGCTGCA CAGACAGACT TGGGAACGAG 1920 GGAATGTCAG TGTGGCAGAG CTGTAGCTGC CTCGGAGCAG CACTATGGGA CCTTAGGCAG 1980 GGCCAGGTGG GCAGGTACAC AGTGACAGCA GGGGGATGCT GGGACCAGGT TCTGGGTGGC 2040 GACGTGGCCT TCCACCTTCT CACTCCTTTG CCATATATGC TGCAGCCCGG TGATGTCTGT 2100 GGCACGAGTT TTAAAAAACT CAACTAATTG 2130
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