| Tag | Content |
|---|
EnhancerAtlas ID | HS041-00040 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr1:1004840-1006060 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr1:1005572-1005583 | TGGGTGTGGCC | - | 6.62 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_24070 | chr1:1002554-1005867 | Colon_Crypt_2 | | SE_24817 | chr1:1002490-1006081 | Colon_Crypt_3 | | SE_27529 | chr1:1001798-1011077 | Esophagus | | SE_34539 | chr1:1004454-1006480 | HCT-116 | | SE_41944 | chr1:1001963-1005965 | LNCaP | | SE_58139 | chr1:1004812-1005267 | VACO_9m | | SE_65935 | chr1:1001682-1006445 | Pancreatic_islets |
|
| | 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 |
| GH01I001066 | chr1 | 1001837 | 1006486 |
|
Enhancer Sequence | CGTGGGCGCC GCCCCCCGCT AATCGGGTTG CAGCCCCCGG CTCCCCGGGC ATCCCCGGTG 60
TGAGTGGAGC GCCGGGGCCG GTCCGGAGTC CTCTGGGAGG GACTGGGACG TGCGGGGTGC 120
AGGGCTGAGC CGCTGCTCCG CGCGCAGAAC CCCGCAGCCC TGGGACGGCG AGGACGCGAA 180
CCTGCGGAGC CGCGGGTGTC TGAGGAGCCG CAGGGAACCC CCGGCCTAGC CGCGCCCGCG 240
TGTGGCCGGA GCTGCGGGCC GGGACTGTGT CCAGGACAGA GCCACAAGCT TGTCCCCAGC 300
TCAGGGAGGT CCAGGGGCGG CAGAGGGAGC GACAGGCTGC GAAGCCCACC GGTGACCACG 360
TGTGAACCCG CGTGCGCCCC CAGCTCGGCC ACTCCGTGCG GGTCTGCCCT CACCGCAGCT 420
CCGGCCTGCC GGCCCTGCCT GCTCCCGTGG TCTGGGATGT GGCCCCGGTG AGGACCCGGC 480
CCCATCAGGC ACAGGGTGGA TGTCTGTGGA GTGAGGTGTG TGTGACATAT TCATGTGACC 540
ACCCGTGCAG CGTCACGCGC CTGGCCCTGC CGATGACAAG GGTGTGGGCC TGCGTGGGCA 600
TGACTGTGTG TGTGACACAG AGTGATGTTG CTGTGACCCG TGGCTGCACT CCCCACATCA 660
CCGGCTTTCA CAGCCTTCCG GTAAAGTGCT GTGTTCTCCC TTCTGTGTCT TCGCTGGGAC 720
CTGGGGCAAG GGTGGGTGTG GCCCCCACAG CTGGAGTCAG CTTCTGTGGG GCCTTCCCGA 780
GCCCTCCCCA CCCTGGACCA GAGGCCCAGC TGGTTGGAGC AGGAAGTACC TGGGCTCTGG 840
GGTCAGGGAT GGGAAGGCTG AGGAGGCCTG CGTGAGCTGG ACCTGGCCTG GGCCCTCCTG 900
GCCGTGCCTG CCTGGTGGTG CAGGATTCCT GGGGCTGATG ACAGACGGGG TAGGGCTGGG 960
GTTGGCGAGC CTCCTGCCGA TACCTCACGT AGCTGACCTC TGACTCTTCC CCAGCCAGGC 1020
TGGCCCTGGG AGTTGCCGGA GAGTCAGTGG ATCTGCAGGC TGCACGCTGG CTGTTACCTT 1080
TGCTTCTGGG TTCCCACAGG GGTCATGGTT CTGTGGTTCT CCAGTCAGGG ACCCTAGCAG 1140
GGCCATGGGG CGTGACTTCC TGGAGGTGTG GCCTAGTATG GCCACGGCAG AGGATGGGGG 1200
AAGAGAAAGG CCCCCTTTGT 1220
|
