EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS052-07612 
Organism
Homo sapiens 
Tissue/cell
Fibroblast_foreskin 
Coordinate
chr11:113961620-113963260 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs17116334chr11113961762hg19
TF binding sites/motifs
Number: 17             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr11:113962325-113962343CCCTCCCTCCCTCCCTCC-6.03
EWSR1-FLI1MA0149.1chr11:113962334-113962352CCTCCCTCCCTTCCTCCC-6.92
EWSR1-FLI1MA0149.1chr11:113962330-113962348CCTCCCTCCCTCCCTTCC-7.08
EWSR1-FLI1MA0149.1chr11:113962346-113962364CCTCCCTTCCTTCCTTCT-7.79
EWSR1-FLI1MA0149.1chr11:113962338-113962356CCTCCCTTCCTCCCTTCC-8.06
EWSR1-FLI1MA0149.1chr11:113962342-113962360CCTTCCTCCCTTCCTTCC-9.83
SP8MA0747.1chr11:113962730-113962742AGTGGGCGTGGG-6.14
ZNF263MA0528.1chr11:113962114-113962135CCCTTCCTCTCCTCCACCCCC-6.44
ZNF263MA0528.1chr11:113962329-113962350CCCTCCCTCCCTCCCTTCCTC-6.54
ZNF263MA0528.1chr11:113961659-113961680TCCTTCTCCACCCCTTCCCCC-6.68
ZNF263MA0528.1chr11:113962338-113962359CCTCCCTTCCTCCCTTCCTTC-6.93
ZNF263MA0528.1chr11:113962325-113962346CCCTCCCTCCCTCCCTCCCTT-7.05
ZNF263MA0528.1chr11:113962111-113962132TTTCCCTTCCTCTCCTCCACC-7.13
ZNF263MA0528.1chr11:113962333-113962354CCCTCCCTCCCTTCCTCCCTT-7.27
ZNF263MA0528.1chr11:113962342-113962363CCTTCCTCCCTTCCTTCCTTC-7.39
ZNF263MA0528.1chr11:113962330-113962351CCTCCCTCCCTCCCTTCCTCC-7.9
ZNF263MA0528.1chr11:113962321-113962342TCCTCCCTCCCTCCCTCCCTC-8.08
Number of super-enhancer constituents: 23             
IDCoordinateTissue/cell
SE_00466chr11:113962169-113964950Adipose_Nuclei
SE_01195chr11:113962225-113963441Adrenal_Gland
SE_01539chr11:113959073-113963612Aorta
SE_03352chr11:113959099-113961849Brain_Angular_Gyrus
SE_03352chr11:113962104-113963649Brain_Angular_Gyrus
SE_04786chr11:113957562-113965982Brain_Cingulate_Gyrus
SE_05774chr11:113956129-113966021Brain_Hippocampus_Middle
SE_06716chr11:113956749-113964920Brain_Hippocampus_Middle_150
SE_07716chr11:113954951-113961943Brain_Inferior_Temporal_Lobe
SE_07716chr11:113961999-113965000Brain_Inferior_Temporal_Lobe
SE_08909chr11:113962535-113962750Brain_Mid_Frontal_Lobe
SE_13900chr11:113962415-113962990CD34_Primary_RO01536
SE_20076chr11:113959170-113962084CD56
SE_20076chr11:113962333-113964458CD56
SE_32314chr11:113962376-113963332Gastric
SE_40584chr11:113958957-113962136Left_Ventricle
SE_40584chr11:113962162-113964592Left_Ventricle
SE_41565chr11:113962469-113962963LNCaP
SE_42095chr11:113958962-113964708Lung
SE_48046chr11:113940997-113964660Psoas_Muscle
SE_48753chr11:113961872-113964478Right_Atrium
SE_51074chr11:113958971-113961896Skeletal_Muscle
SE_51074chr11:113962066-113973010Skeletal_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11113961985113963200
Number: 4             
IDChromosomeStartEnd
GH11I114088chr11113958972113961896
GH11I114093chr11113961923113962122
GH11I114091chr11113962323113963121
GH11I114092chr11113963160113964680
Enhancer Sequence
TTCCACTTAT TTATTTTCCC CTCTGAGTTT CAGATTTCAT CCTTCTCCAC CCCTTCCCCC 60
TGCCCTAAGG TGGGGCTAGT GCAAATCGCA GTGTGTGTGT AGTGGGATGG TTAAAGAGCC 120
GTACATCCTC ACACCTGGTG ACGCAGACTA AGGCAATTAA CCTTCTTTAG TAAAGACCCT 180
TTCAGCTGGG TGCGGTGGGA GGCACTTCGG GAGGCCGAGG TGGAAGGATT GCTTGAGCCC 240
TGGAGTTGGA GACCAGCTTG GGCAGCATGG TGAAACCACC TCTCTAAAAA AATATAAAAA 300
TTAACGGGAC GTTGTGGCAT GCACCTATAG TCCCAGCTAC TTGGGAGGCT GGGGCACGAG 360
AAGTGCTTGA ACCTGAGAGA TGGAGACTGC AGTGAGGCGA GATTGCACCA CTGCACTTCA 420
GCTAGGTGAC AGAGTGGGAC CCTGTCTCAA AACAAAACAA AACAACAACA AAAAAAGCAT 480
GTTTTCCTGT CTTTCCCTTC CTCTCCTCCA CCCCCTGGCA TGAACTCTCA ACTCCTGGCC 540
TGTGGATGTC CGTTTCTATA AATGCTGGTG CTCGGTGGTC ACCGTAGACG TCCGAGCAGC 600
CCCTGGGGCT TTGGCTTGTG TTTTCTCTGT ACTTGTGAGG GTGGTTGCCA CTTCTGGCCT 660
TCTTTGTGCT TTCTTTTTCT TTCCTTTCCC CAATCTTTTG TTCCTCCCTC CCTCCCTCCC 720
TCCCTTCCTC CCTTCCTTCC TTCTGCTTTC CTGTTTAAAG TATATGGCTG CACCTAGCAT 780
GACACAGTTC CTATTTATTC CTCAGACTTG CTGGGACAGT CTCCTCTGTA TGCGGCGACT 840
GAGGGTGGGT TCCAGTGCCC CAGCCCACTC CCCTTCCCCT TGTTTTTGTC CACTTGGCTG 900
GACAAAGAGA ACAAAACCAA ATGGCCTCCC CTCCCCCTCT CCTAAGCCGG TCAAGCAGTG 960
GTATTCTGGG ATGATTTTCC CTGCAACCAT TTAAACAAGT GCTTTGATGC TTACGAGTCA 1020
TTGGAATGAC CAGGCCTGTG CGCCCCTTCT CACTGACACC CTTAGACCAG GCTGGGCCTC 1080
ACCCTTTTGT CTTGCTGCCC CTCGGTGCCC AGTGGGCGTG GGCAGTAGGA CTGAGCAGAG 1140
GGGCCGAGGC TGTGCTGGCC GGCAGCTCTG TTACAGTAGA GTGGAAGGAG GTCCCGGCCA 1200
GAGGGGCAGG TCAAACAGGC CTCTTTTATT TACAGTGCTC TCTTTCACGG CCTCACTGAA 1260
ACAGGAGACC CGAGAGGCTC CGGTGAAAGG GCACTGTGTT TGTGCATTCA GGCCTTCCAG 1320
GGCTGGCTAC AAAGGTGGGG GCACCCGGAG CACTGAAGGG GCTTTTTGTC ATTGGCAGTT 1380
TGGCTTAGGG GAGAAGCGAG GGAGAGCCAG TGTGGGAGCC GCCTCTAGGA TTGTGAGCAA 1440
GTGCCTGTTT AGACAGCTCC ACGCTGCTCC TTAAAACCTA TTTTGTGGTC TGGGGTTGGG 1500
GCGGGGGCAC ACTGCCTCGA TCCTCTTGTT GTGTGGAGCA AAGTGATTCC TCTCTTCTTG 1560
TGTTCTCCAG ATGGTTCCGT TGTCCTCACA TCCATTGTGG TTGAGGATAC AGTGCAGAGA 1620
AGACCCCGCT GTCCTCTGCT 1640