Tag | Content |
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EnhancerAtlas ID | HS048-32747 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr6:140028980-140030580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr6:140030124-140030135 | TTTGACCTTGA | - | 6.14 | Esrra | MA0592.2 | chr6:140030125-140030136 | TTGACCTTGAA | - | 6.14 |
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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 |
GH06I139707 | chr6 | 140028689 | 140031197 |
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Enhancer Sequence | CCTGAAAAGT TGGGTTGCTG TTGATATCCT CGTGGTCCAT GCCCAACAGG TCCTCAAATG 60 TGGATGGCTC CGTTGTCCCA ATACCAAGTA GGCTATGAAT GGTGTTTGCC TGAGCTGGGA 120 GCGCTAGTTC CTAGGATCTA GCTTTCTGGA TTCACCACAC AGCCATATCT TTTGAAATTT 180 TTTGCTACCT TTCAAAGTAC TGCAAGAAAG TGAGACATGT ACCCTCACCA CCAATGGGAC 240 CTTCCATTCT ATTCCCTTCC TAGGAAAACA TTGAGCTTCC CACTGTGGCT TCCTACCTTT 300 CCTTCCCAAA GCATCCACCT ATTTTCTTGC CTCTCCATGA ACCATAGCTT AATCCCCACA 360 AGGAATCCAG GCTTTCTGTG CAAAAGTCAG GAAGGAGACA GGAACAGGAA GAGGACAGGG 420 ATGTTTTCAG GAAATGTCTG TAACAAAAAT CTCCACTGAG ACCAGCAGCA CAGAGCACCT 480 GACTGCCTTT TTTTTTGGAA TGGGATGGTG GTAGGTAGGA ACAAAAAAAA TGCAGGGATA 540 AACAAAACCT AAATTAATGT CTCAATTTGT TAACCCATTG CACTATCAGA GTACAGACTC 600 CTGGCAAGCA GATGCCAAAA TTGGTAACAT GTCCAGATTG GCTCCAGTCC AGCAGAAGTT 660 CAATTGTTGA AGAACATGTA TAAAGTCTTC TTAAATACTG TTTGGTCACA CCCATTCATT 720 AGTCTGGGCA TACTTCCTTT AGGGAGTACC AACCAGTGCC TTCTTTATTT TATATTAAGG 780 GTCACAGAGG ATGAAGTTTG GTGAGGCACT TCAGGGGGAT TTTCCAATGG GTTTGAATGA 840 GTCTTAGAGA AAATTGTATA CTCCAAACTC CTTGGAGAAG AGCTTCCTGG GATAAATGTT 900 AAATCTGTAT CAGAACAGAG CACAGCTCTT GTCACTGTTT GGTGCCTGGG TCTGCTGCTG 960 GAAAATTCCT CTTGCCTTAT GCTATCAAGT GAGCTAGCTA AATTCTGGAG AAAGCTGCTC 1020 ATAAAACTGA TAAGAGCCCT CTGTTAAACA ACCTAATTTG AACTTTATCC CAGAGACCTT 1080 GAGAAACAGG GTCTGCACTT TTATAATCCA AGAATTGAAT ATGGTCCTGC ACAGTTGGGT 1140 AACATTTGAC CTTGAAACGT CGTTCTAAAA GTCGTGTTTC CCCCTTGCTG GCTTTGCTGT 1200 TATCTGTGCA TCAGTGAACA CTTTATCATA GTAACGCTTC AGGAATGTGC AGAATAGTTG 1260 AGGAGCTTGA ATGCCACAGC AGTTTCAAGT ATGCTGGGCT CTTGCTACCA GCTCACTGGG 1320 TCGGTCGCTA GAAGACTGCT ATAGCACATA TGCTGCAGAA CTGACGTTCA TTACCAGGTC 1380 ACTTTCAAAG TGTTGGCTAG CAAGTCTGTA GTTAGTTCTT ATTTTTCTCC TATGATTTCT 1440 GTTTTCAACA AATTTGCAGT CCATTTGGAC AGGTAGAATA AACAGGGCAA ATAAAACCAT 1500 AGAAGAATTA TTGAGTTCTT CCTACTTCTT ATTATACGAA GGGCATGGTA TGCATTTTCC 1560 CCTTTAACAT AACATGCAAC ATCCAACAGT CTGGAAAGGT 1600
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