EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS080-29921 
Organism
Homo sapiens 
Tissue/cell
H9 
Coordinate
chr5:176525230-176526960 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs183041chr5176526270hg19
TF binding sites/motifs
Number: 25             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr5:176526907-176526925TCTTCCTTCCTTCCTTCC-10.05
EWSR1-FLI1MA0149.1chr5:176526919-176526937CCTTCCTTCTTCCCTCCC-6.84
EWSR1-FLI1MA0149.1chr5:176526899-176526917CCTTCTTTTCTTCCTTCC-7.71
EWSR1-FLI1MA0149.1chr5:176526895-176526913CCTTCCTTCTTTTCTTCC-8.01
EWSR1-FLI1MA0149.1chr5:176526915-176526933CCTTCCTTCCTTCTTCCC-8.13
EWSR1-FLI1MA0149.1chr5:176526891-176526909CCTTCCTTCCTTCTTTTC-8.32
EWSR1-FLI1MA0149.1chr5:176526903-176526921CTTTTCTTCCTTCCTTCC-8.5
EWSR1-FLI1MA0149.1chr5:176526883-176526901TTTTCCTTCCTTCCTTCC-9.07
EWSR1-FLI1MA0149.1chr5:176526887-176526905CCTTCCTTCCTTCCTTCT-9.09
EWSR1-FLI1MA0149.1chr5:176526911-176526929CCTTCCTTCCTTCCTTCT-9.09
Myod1MA0499.1chr5:176525420-176525433TGCAGCTGTCCCC+7.12
Myod1MA0499.1chr5:176525633-176525646TGCAGCTGTCCCT+7.82
MyogMA0500.1chr5:176525419-176525430CTGCAGCTGTC-6.62
MyogMA0500.1chr5:176525632-176525643CTGCAGCTGTC-6.62
Tcf12MA0521.1chr5:176525419-176525430CTGCAGCTGTC-6.14
Tcf12MA0521.1chr5:176525632-176525643CTGCAGCTGTC-6.14
ZNF263MA0528.1chr5:176526914-176526935TCCTTCCTTCCTTCTTCCCTC-6.07
ZNF263MA0528.1chr5:176526899-176526920CCTTCTTTTCTTCCTTCCTTC-6.09
ZNF263MA0528.1chr5:176526918-176526939TCCTTCCTTCTTCCCTCCCTC-6.3
ZNF263MA0528.1chr5:176526910-176526931TCCTTCCTTCCTTCCTTCTTC-6.48
ZNF263MA0528.1chr5:176526883-176526904TTTTCCTTCCTTCCTTCCTTC-6.56
ZNF263MA0528.1chr5:176526907-176526928TCTTCCTTCCTTCCTTCCTTC-7.03
ZNF263MA0528.1chr5:176526895-176526916CCTTCCTTCTTTTCTTCCTTC-7.15
ZfxMA0146.2chr5:176526231-176526245GAGGCCGAGGCGGG-6.01
ZfxMA0146.2chr5:176525519-176525533TAGGCCGCGGCCCG-6.21
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_30460chr5:176524131-176528574Fetal_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr5176525400176526462
chr5176526460176526848
Number: 1             
IDChromosomeStartEnd
GH05I177093chr5176520362176528755
Enhancer Sequence
CCAGGCCATG GGCTCCGCCA CCTCCACTGC CCCAGGAGCC AGTGTGTGCC TATCTGGGTC 60
CGCCTGTCCC ACCAGCCCCA TCTTGTGTCT GCGACAGTGT GAATGAGTAT TAATGGGCTG 120
AGTCCGCATT GCACTATACA CGGTGGGACT CCTGTACCCT CTGCACATGT GTGTGTGTGC 180
ATGTGTGCCC TGCAGCTGTC CCCAAGGGAG CTGGCAGCCC CCCTCCCCCA TCTGCTCAGC 240
ATTAACCAAG CTGACCGTTA ACACAGCATG AAAATCTGAG AGCCAGCCTT AGGCCGCGGC 300
CCGCTCCCAC GCTCTGCCGG CTCAGGCTGG GGGCTTGTGG AGGCCATGCC CGCCCCGCCC 360
TGGCCAGTCT CCCGGGCAGC AGCTGGTTGC CGCCCGCCTG GGCTGCAGCT GTCCCTGCCT 420
GCCTGGTCTT CCACTGAGGA GCCGTCACAG CCCTGTACTC AGAGCTCCTC AGAGTGAGCA 480
GCTTCTCAAG GCTCTGAGCC TGGAACCTCC TTCCCTGGCC CCATCCTGGC ACGTACTGCT 540
ACTCCCCAGC CCCTGAGCCT TGAGTGGGCC ATGGGGGGCC CAGGCATGGT GTCTGACCCA 600
GCACTTGGCA CTCTCCTGTC CTTTTCCTTA CAGGCCTCAG GCTGGGACAG GACTGCCCAA 660
CCAGGACAGC CTTCATGGAG GCCATCGGGA TTGCCCCCGT CTGCCCCCAG GGAGTGGTGG 720
CTGAAAATGC ATATGCGGTC AGAGGGGTCA GACAGAGGGA TTGGAGGCTG GGGCCTCCTT 780
GGAAGACTGA GCGTCAGCTC ATGATTGTTT ATCCTCACTC TGGGCTCCTC CCAGCTCTCA 840
GCATAGCCTC TCCAGCTGAC GGTATCCCAC ACAGAACTCA TCTTACCCCC AGAACTGTAC 900
CTCCTCCAGG GCAGGAACCA GGGAGTCACC TGACTACTTC CCTCAAGAAC CCTGTTCCAG 960
GCCAGGTGCG GCAGCTCACC CCTGTAATCC CAGCACTTTG GGAGGCCGAG GCGGGCGGAT 1020
CACCTGAGGT CAAGAATTCG AGACCATTCT GGACAACATG GCAAAACCCT GTCTCTACTA 1080
AAAAATACAA AAATTAGCCG GGCATAGTGG GGCACACCTG TAGTCCCAGC TACTCAGGAG 1140
GCTGAGGCAG GAGAATCATT TGAATCTGGG AGGCGAGGGT TGCAGTGAAC CGAGATCGTG 1200
CCAGCCTGGG CTAGGGAGCA AGGCTCTGTC GCAAAAAAAA AAAAAAAACA ACCCTATTCC 1260
CTCATGCGCT TCCACGGTCC AGCGTGGCTC CTGAGGCCAG CACTGCCACC TCTCTGATAA 1320
TACTGTCTTT GCCCATGAGT AGGGTGCACC TGTCCCGCCT GCCTCCTGGG GCGTAGGGTT 1380
TAGGAGGAAG CACGTGCAGA TGCACATAGG CTTGGGGGAG GGTGTGATGC GGAGGCCCAT 1440
GGGTTGGGCT GCGGTGCTTC CCTGGGAGCC GGTGCTGGGG CTTTTGTGTC CCTGAGTGCC 1500
CCCCTCCGAG CCCTAGGTAT CCAGCCTCCC TTTTGCTCCC TCCCCTGCAG GTGGCTCCAG 1560
AGGTAGCTTC CAAAAGCAGA CTGGGTTTAT GCTCCCTCCT GCTCTCAAAG ACCCCCACTA 1620
ACTCCCGAAA GCCCCCAGAC TGACCAACTT TCTTTTTCCT TCCTTCCTTC CTTCTTTTCT 1680
TCCTTCCTTC CTTCCTTCTT CCCTCCCTCT CTCTCTTTCT TTCTTTTTCT 1730