Tag | Content |
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EnhancerAtlas ID | HS061-19551 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr5:60615160-60616160 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr5:60616011-60616031 | TTGTGGGGGGTGGGTGGTTG | - | 6.17 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_23393 | chr5:60614822-60616675 | Colon_Crypt_1 | SE_24321 | chr5:60614883-60615358 | Colon_Crypt_2 | SE_24321 | chr5:60615370-60616575 | Colon_Crypt_2 | SE_24851 | chr5:60614658-60619493 | Colon_Crypt_3 | SE_32008 | chr5:60615031-60616546 | Gastric | SE_38270 | chr5:60613797-60616170 | HUVEC | SE_50923 | chr5:60614291-60615379 | Sigmoid_Colon | SE_50923 | chr5:60615388-60617771 | Sigmoid_Colon | SE_54313 | chr5:60614427-60616595 | Spleen |
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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 |
GH05I061318 | chr5 | 60614074 | 60616626 |
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Enhancer Sequence | TTTCAGCCCA AGAGTGCACT GCCAGAGGCA TAACACCTCC CTTGGTGGGG ACCTTTGTTG 60 GCAGCATTCT AAAATGAATT CATAGGACTG TTCTCTGATT TTCAACTTTG CTTTTGATAC 120 AAGGTCTGTG AATGTTTAGT TGACAATACG TGTGCGCCTC TCTCATTTCC TGTTTTTAAG 180 GGCTGCACTT AATTTATTTG AAAGGGTGGA ATATTTTAAA TTACAATTCA GCAGTTTTAC 240 TAAGGAAGGC TGTAAAACAC AATGAGCAAG GAGTTTTACT TCCTCCTTCC AACTGCTACT 300 CCCTGTTTTG AAATCTTGAT GTCCTCCAAT CAATGGGAAT GACTTTAACT TACACTGTAA 360 CATTTTTAAC AGCAACCACG CCATGGCTGG AGCTGCAGAG GGGCATGGGA TTCCTGCACA 420 CTGTAATTCC ATTTTTCCAG ACGCCTTATT AGTACACGGA ATGCGTCTGC CTGTGCTTGA 480 TATTGTTCTA TCTTGTTAAG TCCCCTCCCC CAGGCAGAGC ATTTGGATTG GTTAAGGAAT 540 ACAGTCGCTT AGCCAATCAA GTGAAACCTT TCTCCTGCAA CCCTAGCAAC ACCTGTCATT 600 GACAAATGTT AAGAGAAAAC CCCTGACAAA CCCAACCAGC CCTTGAAAAT GGTCCCTGTC 660 AAGGGCAAGT AGGGCTACTC CTACCCACAG AGCACTTTCT GTGGCCAGAG GAGTTAGTGG 720 TTTGTATCAG ACCTGCAAAA ACAGAACCTG GATGTGGCTG CAGGTGCTTG AGTCTAGGGC 780 CCTATTCCGA TCTGCTGTCA ATTTCAGCGA AACTGACTTT TGTTAGCCAA AGCCGGTGTT 840 GGAGCTTGGG GTTGTGGGGG GTGGGTGGTT GTCTATGGTG GGGTGGCAGC CGGGTAGTGT 900 GCTCATATTC TCCCATACCA ACCAGACCCC CATACCCACC AGAATATTTT CAGTGGCTGG 960 AGGAAGAGTT CACATACAAC TTCGGCTCCA GGGTCACACT 1000
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