| Tag | Content |
|---|
EnhancerAtlas ID | HS095-11664 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr16:72046470-72048000 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr16:72046526-72046537 | GCTTCCCGCCC | - | 6.02 |
|
| | 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 |
| GH16I072012 | chr16 | 72046490 | 72048659 |
|
Enhancer Sequence | GTCACACAGC TAGGAGGTAG CAGGACCAGG ATTCAAACCC ACAGAGTCTG ACGCTGGCTT 60
CCCGCCCCTT GGCCACTGTC CTGCCTTGCT GAGGTCGTGG GTAGCTCAGT CTTCCCCTCA 120
GCTAAATGGG GAAGCTGCCA GAGTCATTAA GCACTGGTGA GAGGCAGGAG CATCGTGTCC 180
CAGCCTCACT CAGCCACGTG TTCAGCACAC GGGCCCTCTC CATATGCTTG AAATCTTTGG 240
CCTAGAGTCC CAGGAAAGCC TCTAGGGCAG GAAGAGGGTG TGTAGGCAGA AGTGTAGATA 300
CAGCCTCTGA CTGCAGAGGC CAGTGTCAGC GGAAGGCTAA GGGCCTCTGT TTCATGTGAC 360
CTTCCGGGCT TAGTGCAGCA AACCGAATAA AAGAGTCCCC ATCCTCATGG AAGCTGCTTC 420
CTCATGGAAG CCTTGGCAGT TTCCTTTCGA GAGGCTTCTT ACCAAATGGG AGGACATCAG 480
AATGATGAGT GTGAAAATGC AAACAAGAAG CCCTCAGAAC TCTGGTGGGA AGGGTCACTG 540
TTATAAATTA AAGGGGCCTT CACCGCATTT TCTCTTCCTA CCTTAGACTC CTCTTCACTA 600
TCTGATTATA TGGTGTTGAG CAGACGTGTC ATTTCCCCTG ACTGGCCATG CTCACACACT 660
AACAGGCACT GTAGGCTCAG AAAGAGCACT CCGTTAAGGT GTCCTCACCT CAGACTGCTA 720
GTTTGAGAGC CCTGGAACCA GTGTAAAATG GGAGTGAATA ATGAGTGGGG TGCAGAGATG 780
GGGTGAATTT AGAAGGAAGT GCGGGGTGCC TGAGGGTGCA AGCTGTGTCT GTATAAACAC 840
AGATGACAGA GACAGGCAAA CCTGACCTCT GAGGTGTTGT CCTCAACACC TCTGCGTGGG 900
CCCACACTTG CAGCAGCTCA TTTAGAATGT GACTCAGACT TTTTAACCGG TAACCAGGAT 960
TCTTGATTTC ACAACTTTCC TGGTTTGGCT CTCCACCCTT CACCTATGTC AGGCATGTTA 1020
GAATCCCCCG GGGGTGCACT TGGAATATTC AGATGCCCTG GCCTGGTGCC AGACCAGTTT 1080
CACCGCCACA TCTGAGAGCA GGACCTGAAA GCTGCCAGGG GCCTTTGTGG TGCAGCTGGA 1140
GCTGAGAACC ACGGTCCTGG AGGAAGGCCC CTACACATCT TGCCTACCAG TCTCCTGAGG 1200
TGCTGTGAGC ATTCTCACCT TCATTTGTTG CTCTTCCTTC TTGGAGCATC TCTCTTAATC 1260
CCCTGCTTCC AGGATCCGAC CGTGTTCACC CCGGGAGGCC TTTGCTAGTC TCCTGAAAGG 1320
TCGCTGGAGC CCATCAGTCA GTTCTGCCCA GCTGAACATC TTCCTTCCTC TGGTTCCCCG 1380
TGGGAGGCTG GGGGACGTGG CTGGGGCTTC TTGCCAGCCC GGATGAGGAG GGACACAGCT 1440
GGAGCTGATG TTTATTAAGC TGATTAAAGG GTTTTGCTGC TTGACACGCC TTGGTTTCAG 1500
GGAAGCACTA TCTAGGGCCT GACACCAGCG 1530
|
