| Tag | Content |
|---|
EnhancerAtlas ID | HS095-16704 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr2:107501530-107502540 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chr2:107501906-107501922 | AATTCCTGGAAAGCAC | - | 7.42 | | BCL6B | MA0731.1 | chr2:107501904-107501921 | TAAATTCCTGGAAAGCA | - | 7.48 | | ESR2 | MA0258.2 | chr2:107501655-107501670 | GGGTCAGCATGCCCC | + | 6.3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AAAAGGGAAG CATCAAAGTA ACCAGCATGG GGTTTTTCAA GTGTGCAGAA AGTTCTCTAA 60
ATACAAAATG TGCTTCCAGC CCACCAAAGA CCCCCCTCAC CCAAGCAGGC AGTCCTCGGC 120
GAGGAGGGTC AGCATGCCCC TTTATGGTCA GAACGGCAGT GGTGCAAAAG ACAATGATTT 180
CAACCAAATA TGGTTTGCCT CTCGCCAAAT TTTTCGCATG TCCAATAAAA ATAAGTTCAC 240
AAAAATCCAG CCAAGCATTA CTTTCCCCCC AAAAGTGCTT CTCAGATTAC AAAACAGCTT 300
TGAAAGTTCA GCCTGACAAA ACAAATATGG TACTAGGAGG AGAGACCTGG AAGGCAATCA 360
CAAAAAGTCT CATTTAAATT CCTGGAAAGC ACAGCTTCTC CAAACACAGC TATTCAGCTC 420
TTTGGAAGGC AGCACTTGCG GGAGCCATTG AGTTTAACTT CACTCAGTCC CCCAACACAG 480
AACCGGCAAA TCCGAATGAG ATGGACGTCA CACTCCCTAC TCAAAAGAAT GCATCAAATA 540
TCCACTCCGT AACACCGCGG AAAGTAAACC CAAAAGCGGA GTTTGCCGCC TGCCAACTAC 600
ATAAGAATTA ACACTCGGGT ATTTAGGATT CTAAAGATCC CTACTACCCC AAACATTATA 660
GCCACAGAGA ACCAGAAATG AACAGAACAC ACTTTAACCT TTAAGAAGTG CAGTTTTGTA 720
CGGGGGTTGG CTGAAGAAAG ACAAAAATCT TCACTCCCTT CCAGAGCCAA AAGAGCCAAA 780
ATAAAAGATC ACCTTTACTG AGCCACAGGG GCACAACTGT ATCCGCCCGT CCCCAAAGCG 840
CAAGCCGTCC TCCCGTTCGC TTCTCCAGAA TTTCCTGCTT TTCCCCAAAC CACCTTCAAC 900
ATTCCCCACA CACGGGTCTC GCTCCTAAAC ACGGAGTGTA ACTCCGCGCA CAGCAGCGCG 960
GAGGCTGCAG CGCCACCAAG AAAGGCGTCG CCAACCCTTA CCCAGTGCCC 1010
|
