| Tag | Content |
|---|
EnhancerAtlas ID | HS104-23639 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr16:70510140-70511670 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROD2 | MA0668.1 | chr16:70510375-70510385 | GCCATATGGT | + | 6.02 | | NR2C2 | MA0504.1 | chr16:70511593-70511608 | GAGGGGCAGAGGTCA | + | 6.52 | | Nr2f6(var.2) | MA0728.1 | chr16:70511305-70511320 | TGAACTCCTGACCTC | - | 6.22 | | Zfx | MA0146.2 | chr16:70510149-70510163 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 70510201 | 70510773 | | chr16 | 70511298 | 70511640 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I070474 | chr16 | 70508755 | 70511590 |
|
Enhancer Sequence | CGTGATCCGC CCGCCTCGGC CTCCCAAAGT GCTGGGATTA CAGGCGTGAG CCACCGCGCC 60
CGGCCTGTGC TGTGCCTCTC ATGCTTGTTG GAACCAGGTG CTGTGCTTCG TGACTGTGCC 120
TTTCCAGGGC TGTGCTGGGG TAGGGCTGGG CAGAGCTGCT TTGGACCTTC CGCCTGTCCT 180
GGCATCGTGC CCTTACTTGA GATATGATCA CCTGTGCCCC CGCCCCCACC CCCTGGCCAT 240
ATGGTGGGAC AGCAAGAGCC CAACAATGAC TATGATCTAA TGAATGTCAC CAGCGCCAGG 300
CTTCTCACTC CTCCTGGCCA CCGAGCCCCC TGGAACCCAT GGCCAGTGTA GAGCAGCTAC 360
AGCTTGTCTG GTTTCAGGTC CACCTCAGGG TGTCAGGTCC CGTCTCCAGC ACACCCCTGG 420
AAAGAAACTG CTGCAAAGGC CTACTGAAGC CTGACTGTGG TGTTTTCTGT CACTCTGCAG 480
CTCAAGCCTC ACATTTCACT GTAGTGACTC ATATCCCATA ATCGGTAGTC ATTAGCAAAA 540
GGAGCAGATG GGGAAGCATT TTCAGTTTTC TTTTGAGGTG TACCATTCAA GTTCTACATT 600
TGGCCAACGG AAAACTATTT GTTGAGAACC CACTCTGTGG GGCCCCAGGG ATAAAATGAG 660
CAAAAATGGG GTCCCTGCCC TCAAAAGTCC TGTGGTCTCC TGGAGACAGA CATTAATCAA 720
TAACTACTCA GGTGCATGTG TATTACAAAC TGTGCCAAGT GCTTTGAAGC AGAGGGGCAC 780
AGTTAAGTCT TGACATTTCA AGACTTAGCC ACTTTGCAAC TACCAGGTTT TGGCTGCAAA 840
GTTCCAGATG GCTTCTGTCT TTTGCATTTC ATACTTTAAA CCCTTGCAGG CCCTTCCCTA 900
ACTATCAAGG GCCTGTCCCA GAAGCAACTC AAGTTTTGTT ATTTTTAATT TTTTTTTATT 960
TTTGAGATGG AGTCTAGCTC TGTCACCCAG ATTGGAGTGC AGTGGTGCGA TCTCAGCCCA 1020
CTGCAACCTC TACCTCCCGG GTTCAAGAGA TTCTCCTGCC TCAGCCTCCC AGGTAGCTGG 1080
GATTACAGGT GCCTGCCACC ATGCCCAGCT AATTTTTTGT ATTTTTAGTA GAGATGGGGT 1140
TTCACTGTGT TGGCCAGGCT CGTCTTGAAC TCCTGACCTC ATGATCCGCC TGCCTTGGCC 1200
TCCCAAAGTG CTGGGATTAC AAGCGTGAGC CACCATGCCC GGACTAGTTT TGTTATTTTT 1260
ATGCAGCTAC AAGGAGGAAA ATGATACATA CCTTTCATTA CTGAAGATGG AAAGATGTGT 1320
AAGTTAGATA AGAGAAAAAC AGATCCTGAT GACCTTCCTT CCAACATAAA CCACCTGTCA 1380
GAAGACGGTG CAGGGAGACT CAGGCCAAAG GGAAGGTATC TGTCAGCCTC TCCTCTGACT 1440
AAAACTCCCC TAGGAGGGGC AGAGGTCAGT GTAAAATATG TATTTTTTGA GACAGAGTCT 1500
CACATTGTCA CCCAGGCTGG AGTGCAGTGG 1530
|
