EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS092-24550 
Organism
Homo sapiens 
Tissue/cell
HFF 
Coordinate
chr2:112250480-112251760 
Target genes
Number: 8             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs138308793chr2112250758hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr2:112250841-112250853AAAAAAACAATC-6.44
Nfe2l2MA0150.2chr2:112251535-112251550TGCTGACTCATTATT-6.19
Number of super-enhancer constituents: 46             
IDCoordinateTissue/cell
SE_00172chr2:112245156-112256428Adipose_Nuclei
SE_01307chr2:112249522-112251663Adrenal_Gland
SE_01980chr2:112249536-112253191Aorta
SE_02250chr2:112246503-112256255Astrocytes
SE_09255chr2:112242322-112254579CD14
SE_11821chr2:112245569-112253926CD3
SE_13188chr2:112250048-112253658CD34_Primary_RO01480
SE_13332chr2:112246928-112254907CD34_Primary_RO01536
SE_14312chr2:112249042-112254777CD34_Primary_RO01549
SE_14375chr2:112242883-112255469CD4_Memory_Primary_7pool
SE_15396chr2:112247191-112253574CD4_Memory_Primary_8pool
SE_16282chr2:112246460-112254339CD4_Naive_Primary_8pool
SE_16917chr2:112248128-112253231CD4p_CD225int_CD127p_Tmem
SE_17781chr2:112242510-112254358CD4p_CD25-_CD45ROp_Memory
SE_18238chr2:112242335-112255432CD4p_CD25-_Il17-_PMAstim_Th
SE_19110chr2:112243711-112254403CD4p_CD25-_Il17p_PMAstim_Th17
SE_19985chr2:112242474-112254362CD56
SE_20734chr2:112242380-112254532CD8_Memory_7pool
SE_22092chr2:112247584-112253444CD8_Naive_8pool
SE_22299chr2:112242383-112254936CD8_primiary
SE_25382chr2:112236252-112254103DND41
SE_25821chr2:112246354-112256327Duodenum_Smooth_Muscle
SE_27273chr2:112248093-112254583Esophagus
SE_30074chr2:112249847-112256216Fetal_Muscle
SE_31329chr2:112250186-112253680Fetal_Thymus
SE_34722chr2:112246590-112256403HeLa
SE_36533chr2:112249648-112256176HMEC
SE_36949chr2:112245538-112256379HSMMtube
SE_38019chr2:112245049-112255663HUVEC
SE_38854chr2:112242450-112258192IMR90
SE_39850chr2:112248124-112254377K562
SE_42753chr2:112248050-112254756Lung
SE_43608chr2:112249704-112253980MM1S
SE_44324chr2:112243463-112259036NHDF-Ad
SE_44769chr2:112246473-112256276NHLF
SE_45566chr2:112242529-112259116Osteoblasts
SE_47156chr2:112242747-112256913Panc1
SE_50094chr2:112242440-112254761Sigmoid_Colon
SE_51387chr2:112247019-112256063Skeletal_Muscle
SE_51721chr2:112248295-112256070Skeletal_Muscle_Myoblast
SE_52359chr2:112245404-112254714Small_Intestine
SE_53336chr2:112246383-112254729Spleen
SE_55797chr2:112245331-112263554u87
SE_58089chr2:112250532-112253746VACO_9m
SE_63507chr2:112248229-112256219HSMM
SE_65208chr2:112250723-112255150NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2112251481112251757
Number: 1             
IDChromosomeStartEnd
GH02I111494chr2112250661112250810
Enhancer Sequence
GTTGGCGTGA AATTGTTAGC CTTGGAAACA ACTGCTGCTC ACATTGGAAC TGCAGGATCT 60
TTCTTGAAAA AGCCATGGAA CTAACTCAAG GGCCACAAGC CCAAATGCCT TCAGAGGGCA 120
GATTAATAAG AGAGTCTAGC AGAGTTAGTG CTGATGGAGT TCCTTCTCCA TCCAGGCCCT 180
GTTCCGGCGG CCGGGCAGAT GCTAACCCAT GGGGACCACA CAGCAGCCCC ACGAGGCTGG 240
CAGGCCCTCA GCCTGGCTTC TGAGCCTCGC TGTAATCGCA CTCTCCAAGC TTTGTGGCAT 300
TAGGGTGTGA CAGGGCCTGA GATCCGGAGA GTGTGGACCC CACCCACAGT TATCTCAACA 360
CAAAAAAACA ATCCTGAGCA GGCCAAACAG AACCTGGTGG GGGATGCCTT CACCAGGGCT 420
GCATCTGGTC CCAGAGCTGC TGGTTTGCAG CCCAACTATT TCGTTTTATT TTTTTAATTT 480
TCTCAATATT TATCTTCTTT TATCTATAAA CGAGTAAGGT TCTGGGGAGG TTTTCTTCCT 540
TGGAATCTTG TTCTCTCATT TTAAGCTGAC TTAATCTTCC CACGCTACAC GTCACATGCA 600
GAGCGCCAAC TTTGAAGTTC ACTCGGTGAC CGACTCTCCC GCCCAATCCC TCGGCGAGGG 660
TGACGTGCAA GCGGAACATC TCAAGGCTCC AGATGCAGGC TCAGCCCTCA GCTGCCCTGG 720
CCTTAATAAA CACTAGATTT TTCATTTCAG AAACTATGTT CAACCTGTTG CCTCAAGACA 780
ACCTAAAAAT CGTCAACATT AGCCAAAGGT TGGAAGCCAA ATGTGTTAGC TCCTGCCTCA 840
GAGACAGATC CCTTAGCAGA GGGGGTCTCT CAGCAGAAGC CCAGAGGAGC TGGGACCCAA 900
GCTGGGAGCT GGTCACTTAC ATAAGGGGGG CATCCTAAGT CGATTTTAAC CCGAGATCCA 960
CCAGCCAAGC CTTCCTACGG GGGGCCGGCC AGCCACCGTG CTGTGCTGAG GAGCAGATTG 1020
AACATTCTCT TAGCTGCTCC AATTTTAGAA TTGGGTGCTG ACTCATTATT AACTCAGGAA 1080
GCCCACACAC TCAAATGACT GTACTGAAAA AGCTCCCTGT CATACCCTGC CTACTGATGT 1140
GTTGCTTTTT AAGCAAATTT GAAAAATGTT TATCATAAGG TATTTATGAC ATTTTAACCG 1200
TTTCATTTAC AGTAACTAGA ACAACATTAA AAAAAAAATG TTTCCTGTAT TTTACTTGAC 1260
AGTAAAGCTA AGCTTCATCG 1280