EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-47690 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr2:219154390-219157180 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs992157chr2219154781hg19
rs2382818chr2219155907hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EsrraMA0592.2chr2:219155549-219155560GTCAAGGTCAT+6.32
EsrrgMA0643.1chr2:219155550-219155560TCAAGGTCAT+6.02
KLF4MA0039.3chr2:219154552-219154563CCACACCCTCC+6.32
ZNF263MA0528.1chr2:219156036-219156057AGAGGAGGCAGGTGAGAAGGA+6.49
ZNF263MA0528.1chr2:219156312-219156333AGAGGAGGGAGAGGAGATGGA+7.23
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_00326chr2:219145665-219158265Adipose_Nuclei
SE_03432chr2:219154454-219157349Brain_Angular_Gyrus
SE_06270chr2:219145735-219164206Brain_Hippocampus_Middle
SE_08985chr2:219155703-219156915Brain_Mid_Frontal_Lobe
SE_10092chr2:219146718-219159598CD14
SE_11206chr2:219145902-219159097CD20
SE_12180chr2:219148529-219157314CD3
SE_14014chr2:219148910-219157816CD34_Primary_RO01536
SE_15197chr2:219146865-219158111CD4_Memory_Primary_7pool
SE_16725chr2:219154813-219157847CD4_Naive_Primary_8pool
SE_17020chr2:219153033-219157989CD4p_CD225int_CD127p_Tmem
SE_17694chr2:219145927-219158488CD4p_CD25-_CD45RAp_Naive
SE_17933chr2:219145740-219158304CD4p_CD25-_CD45ROp_Memory
SE_18906chr2:219145938-219158335CD4p_CD25-_Il17-_PMAstim_Th
SE_19423chr2:219148822-219157978CD4p_CD25-_Il17p_PMAstim_Th17
SE_20197chr2:219154274-219158091CD56
SE_21204chr2:219148412-219158157CD8_Memory_7pool
SE_22529chr2:219146601-219158435CD8_primiary
SE_26022chr2:219146503-219160474Duodenum_Smooth_Muscle
SE_27110chr2:219153196-219162475Esophagus
SE_27658chr2:219148708-219161413Fetal_Intestine
SE_28578chr2:219146925-219161400Fetal_Intestine_Large
SE_30125chr2:219154218-219158006Fetal_Muscle
SE_32283chr2:219154277-219157757Gastric
SE_35648chr2:219153304-219159543HepG2
SE_36018chr2:219146032-219158345HMEC
SE_45286chr2:219154286-219157309NHLF
SE_47526chr2:219154386-219157655Pancreas
SE_50394chr2:219149842-219160653Sigmoid_Colon
SE_51585chr2:219145632-219158203Skeletal_Muscle
SE_52542chr2:219149722-219160735Small_Intestine
SE_57570chr2:219154375-219154848VACO_503
SE_57570chr2:219154969-219157318VACO_503
SE_58066chr2:219154372-219154887VACO_9m
SE_58066chr2:219155603-219157310VACO_9m
SE_64537chr2:219153043-219158397NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr2219156400219156743
chr2219154410219154950
chr2219155683219156025
Enhancer Sequence
TGCCAGTTTC TGATTCTGAA TGAACAGCCT AACAGGAGGC TTCAGGGCAG AATGGCATGG 60
CTCCCCAAGA ACCTACACCA GGGGGTCACT ACTGATGTGC AACTGTTTCC AAGGACATCT 120
TCAGAGGCAG AAGTACATGG CATGTTCTCA GTATGGGGCT GTCCACACCC TCCCAAACTG 180
TCCCCATAAT GCTGTCTGGA CCCTACGGCC AGCTCTTCCT GGGTGATCAG TTACGCCCGA 240
GCTAAACAGT ATATAACACT CTAGGAAAGA AAGAGTAGGA GGCAGGAAGT CCACTGACCT 300
GGGTTCATGA ACTAGCTGCA GGAATCCAGG CAAATGACCT CCCCTGGCCT CCTTTTATCC 360
CTAAATCAGC CCACGTGGGG GAAAGGAGTA GGGACTTGTT TATGGGAGCC ACAGTGGAGA 420
AACAGAATCA CCTAGCCAGG CATTTCCCAG ACTGTTCTAA AGAACACGCC CCAGGAGACG 480
TTAATGAATG AGTGCTGGAA ACAGATGACT CTTGAGAAAC AATCCACACC CCCTTCTTGG 540
AAATTCACAA TGGCATATTC TGCCCCTGAG AAGTCCTGCA GTAAGCAACC CTGTTCAGCT 600
TTGTTTAACC CAGTGTTCCT TCAAACTCCC TTAAGCCTGA GCCACTTTTA TCGAGGCAAA 660
CCTATTAACA CCCTGTGGGA TGCTGACCCA GGCCACCTTT GTATTACAGA CACCCAACCC 720
TGAGAATCAT TCATATCCTA ACTCCTCGTC TCTTATAACC TCTGTGCGTA CACCCAGCTG 780
CCCCTCAGAG CAGTCACATG AAGTACTAGA CATGCCCTCT CACTCTCAGG GGGTCAGCCC 840
AGTGCCAGGA TCTCTGGCGA GGGTCCTCCC CTTCCCCCAT TCCACACAGC TGCTATCCCA 900
CCGTGGGATT TACTGCCAAG GGCCGGGGGA CATATCCAGC TACCACAGAA CCAGGAAACG 960
GGCACCCCTA ACCTCACCTC TGTGCAACGG GGCAAAGCAC AAATCATTAC AGACAAAAGT 1020
GGGAGCTCAT TAATATCTCC CTTCCCACCA ATGGAGGTAC CTGCCACTGT AGCCTGTCGA 1080
CTTCTGGATA TCATTTCTAC TTCAAAACAA GACCCAGGTT TTGGCCTAGA ATCCCAGAAT 1140
CTTAGGGTTG GAAGATTCTG TCAAGGTCAT CCCTTCCACT GTGTCCCCAA CAGAATAGGT 1200
CCAGAAGGCC CATGTCATGA TCAGACATGT TGTTAGCAGA ACTTCTTCCC AGAGAATTGT 1260
ATGAGCTTCC ACTCTCTGGT CGTCCCAGTT CAGCCCTCTG AAAACACACA AGTATGTGTG 1320
TTTCCCTTCT CTGTGGCTTC TGCTTTTTCT GAAAGGCCCA GGGTGAGGCC TGCGGTTGGA 1380
GGTGCTCTGA GGTAGACAGC GTCTGGCTGA GGCACCCATT CCCAGGGGAG GAGGCTGAGC 1440
CCAGGTGGCT ATTACCCCAG CTCATGACAT GAGGCTCTCC CAACACTTAC AGGATAACCC 1500
ATCATTACCT CTCTGAAGGG CTCATTTTTA CAAGTGAGGC CTTGAGGTCA TAGCACAGAA 1560
AGACAGGGCC CCTGACACTG TGGTCCTGCC TCTTCCATTT AAGCTATAAA CTGGTTCTCT 1620
GGATCCTCAT GACTGGAGAG ACAGAGAGAG GAGGCAGGTG AGAAGGAAGT ATGGCTCCCC 1680
CTTTGCGCCA ATAAAGCAGC CCCAGGAGGC ACCTGGCTCC CCTGCCACCA CTGGCCAGCC 1740
CAAAGTCGCC AGCTTGGAAA CCAAAGCTCA CTAATGAGAT GAATATTTCA GAGCCCAGAG 1800
AACTGGACAC CTGAGGGCCC TTCCATGACA TCTGGCTCTG ACCTGCGTTC CCAGGCCTAC 1860
TTATCCCATG TCCAGGGTGC TCAGGTAGAA CCCCAAACTC CTGGGTACCA CGTAGAGGCC 1920
ACAGAGGAGG GAGAGGAGAT GGAGACCCCA TAGGACAAGA ATTGGTGCCG ACCCCACAAG 1980
GCCAGGGCCT GGCCTCCCAG CAGCCTCCCT CTGCTTCCTC CCACTGGTCC CTGGCTCCTG 2040
CCCCAGTCTC TCCACTTGCT TTCCCTTTTC CCGTTTCTCT GTTTTGTTTT CACTCTAACC 2100
CAAAGAAGTC ACGAGGAGGA TGTTACTCCC CTGTAGTTCT GTGAACCCAG CCGGGAAACA 2160
GTGGCTGGAA GTGGGACTGG CAGAGGGCAA AGTCATGGTG ATAGAGGTGG CCACTTCCCC 2220
ATGCCAAACA CTTGAGCTGC TCATTGGCTT CTGCCCCAGC TGCAAGCTAG GACCCCCCCT 2280
TCCCCACCCC TTAAATATTC ACCTGTCTAC ACCGAGACTG GCCTCAGCGC GTGTGGGGGC 2340
AACCTGGGGT CCGTGCCAGG CCCTGGCTGT CTCCCCTCCC TCTTCCCTCT TCTCACCAGC 2400
TGAGGGCCAT GAAAGCCCTC ATCCCACACA GCTGGCCACT CGGGCTGGCA TGGTGGATAG 2460
GCCCTGCGAC AGAGAGGCCA CTCGTGCCCG AAAGAGGGAA CACGAGGACA CCCCCAGACC 2520
CTGGCTCCGC TCACCAGTGC CCACAACACG CTGCTGGGCT CCCAAGGCTA ACCAGGTGCC 2580
ACAGACCCGG CCGCCCACCC GCGCGCCCAG GGAGAGCGAA ACGCCAAGGG CCAGGAGGGG 2640
AGATCCCCAT CTGGAACGGG CTCCTTGGGC CCAGGAGCGG GCAAGCCGGG AGCGCGCTCC 2700
GAAAAGTTTA GGCGCCCCGG CGCATGGCCG CCCCAGCCCT GGACCAGTCC CCACCGCCCA 2760
CAGTCCCCAA CGGCGCCGGC CCCGGCCCCC 2790