| Tag | Content |
|---|
EnhancerAtlas ID | HS095-08779 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr14:23367270-23368380 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr14:23367966-23367984 | GGAAGGCAGGGAGGCAAG | + | 6.41 |
|
| | 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 |
| GH14I022896 | chr14 | 23366207 | 23368602 |
|
Enhancer Sequence | CTTTCCATTA CACGGAAAAG AGGGACTGTG ATATAATTCC ATCCTTCAGG TTTTTACTCA 60
ATTCCCTTCA TGATATGCTC CAGGACTAAA AGTTCACAGG TCAAGCCTCT GCTTCTACTG 120
GTAACTCCTA TCTGGGGGTT GTTGGGAGTC TGAGGAAGCA GGCAGAATTC CTGTGTCAAG 180
AGCACAGCAG TTTAAAGAAC AGGGAGGAAA TGCTGCCACC TTAGTGAATA CAGAAGCATA 240
GACTGGAAGT CAAAAATCAG GTGAGAATCT TTTCTAGAAC TGAAGACTGG TAGGGAAATT 300
CTAACTATGC TGGCAAAGGA TCTAGATCAC AATGTCACCC CTACGCCACC AGCCACCATG 360
TGCAGGTAGA TGTTGAGGGA AGTTTCTTTT ACCTTAAGCT GGGCCCAGAG TCTGTTCACA 420
GCCCGCTTCT CTCCACTCTA ACCACCTCGT ATGGAGGGAT GAGTAACAAG AAGGCACTGA 480
GTCACACACG GACAGCAACT GTCACTCACT AGATACCATC ACCTTATATG GAGTAAGACT 540
GGAAATTGTC TTAGATACGT CCTTACTTCC AACATTGTCT CTCTCCCAGC AAGAGGCTAT 600
GTGAGGAACT AAGAACAAGA AAGAACTGAG GTGGAAGGAT CCGAGTGTAG GAAGGCCAAG 660
GTAGCTAGGG ATGGAAACAT AAGGAAACCA AGCAGAGGAA GGCAGGGAGG CAAGGCCTGT 720
GGATATTTAT AATAGTCTGA AGGAGCCAAG CCAGCCATGA GAAGACCCAG TTCATGGCCT 780
CAGGATGACT AACAAAAACG GTACCCACTG CACTTCTCAA GATACATTAG AAGCCAAATC 840
AATAACTGTA GGGGTGCTGG GTCATAGCCA GCAGCTTCTA CCTAAAAATA GTGCATCCTC 900
CTTCCCTTTT CCCCCGGTCC AGAAAGCAAA CTAGGATAAG ATGGGGGAAG GGATGGGGGT 960
GGTAACCAGG AGAACAGCAA CATCATGTGA GATCTAGGCC TGGAAGAATC AGAAATGCTG 1020
TGGTTTGAAT GTGTCCCCCA AAAGTTCACA TTGGAAATTT GACTCCCAAT GCAACAGTGT 1080
TGAAGATGGG GCTTAATACG AGGTGACTGA 1110
|
