| Tag | Content |
|---|
EnhancerAtlas ID | HS044-10381 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr5:60614980-60616000 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZBTB18 | MA0698.1 | chr5:60614985-60614998 | GAACATCTGGCTT | - | 6.19 |
|
| | 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 |
|
| | 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 |
|
Enhancer Sequence | AGCAGGAACA TCTGGCTTAT TTGCAGTTAG ATTTTCTGCA GGGAGGGTTC AGCCATTGCT 60
ACCATAGCTC TTAGTACCAT AAGGTTTATC TGAATCTCTG AATATCTATG CTCTTGCAAG 120
ATCCAAATTT CCCTTAAAGT TGATATTTGT CTTTCATTTG TTTCCTAATT AGCATTCAGA 180
TTTCAGCCCA AGAGTGCACT GCCAGAGGCA TAACACCTCC CTTGGTGGGG ACCTTTGTTG 240
GCAGCATTCT AAAATGAATT CATAGGACTG TTCTCTGATT TTCAACTTTG CTTTTGATAC 300
AAGGTCTGTG AATGTTTAGT TGACAATACG TGTGCGCCTC TCTCATTTCC TGTTTTTAAG 360
GGCTGCACTT AATTTATTTG AAAGGGTGGA ATATTTTAAA TTACAATTCA GCAGTTTTAC 420
TAAGGAAGGC TGTAAAACAC AATGAGCAAG GAGTTTTACT TCCTCCTTCC AACTGCTACT 480
CCCTGTTTTG AAATCTTGAT GTCCTCCAAT CAATGGGAAT GACTTTAACT TACACTGTAA 540
CATTTTTAAC AGCAACCACG CCATGGCTGG AGCTGCAGAG GGGCATGGGA TTCCTGCACA 600
CTGTAATTCC ATTTTTCCAG ACGCCTTATT AGTACACGGA ATGCGTCTGC CTGTGCTTGA 660
TATTGTTCTA TCTTGTTAAG TCCCCTCCCC CAGGCAGAGC ATTTGGATTG GTTAAGGAAT 720
ACAGTCGCTT AGCCAATCAA GTGAAACCTT TCTCCTGCAA CCCTAGCAAC ACCTGTCATT 780
GACAAATGTT AAGAGAAAAC CCCTGACAAA CCCAACCAGC CCTTGAAAAT GGTCCCTGTC 840
AAGGGCAAGT AGGGCTACTC CTACCCACAG AGCACTTTCT GTGGCCAGAG GAGTTAGTGG 900
TTTGTATCAG ACCTGCAAAA ACAGAACCTG GATGTGGCTG CAGGTGCTTG AGTCTAGGGC 960
CCTATTCCGA TCTGCTGTCA ATTTCAGCGA AACTGACTTT TGTTAGCCAA AGCCGGTGTT 1020
|
