EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS058-02902 
Organism
Homo sapiens 
Tissue/cell
GM10847 
Coordinate
chr16:22201940-22204090 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs145049847chr1622202002hg19
TF binding sites/motifs
Number: 18             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
E2F6MA0471.1chr16:22202295-22202306CCTTCCCGCCC-6.62
EWSR1-FLI1MA0149.1chr16:22203878-22203896ACTTCCTTCCTCTCTTTC-6.37
KLF14MA0740.1chr16:22202286-22202300AGCCACGCCCCTTC+6.1
KLF16MA0741.1chr16:22202164-22202175GCCCCGCCCCC+6.02
KLF16MA0741.1chr16:22202657-22202668GCCCCGCCCCC+6.02
KLF5MA0599.1chr16:22201948-22201958GCCCCGCCCC+6.02
KLF5MA0599.1chr16:22202164-22202174GCCCCGCCCC+6.02
KLF5MA0599.1chr16:22202657-22202667GCCCCGCCCC+6.02
Klf12MA0742.1chr16:22202071-22202086GACCACGCCCTTGAC+6.18
SP1MA0079.4chr16:22202161-22202176CTAGCCCCGCCCCCG+6.13
SP1MA0079.4chr16:22202654-22202669CTGGCCCCGCCCCCT+6.57
SP1MA0079.4chr16:22202284-22202299ATAGCCACGCCCCTT+6.5
SP2MA0516.2chr16:22202344-22202361CTCTGTCCCGCCCCCTG+6.05
SP2MA0516.2chr16:22202653-22202670CCTGGCCCCGCCCCCTC+6.09
SP4MA0685.1chr16:22202161-22202178CTAGCCCCGCCCCCGTT+6.66
SP4MA0685.1chr16:22202284-22202301ATAGCCACGCCCCTTCC+6.93
SP4MA0685.1chr16:22202654-22202671CTGGCCCCGCCCCCTCC+7.25
ZNF263MA0528.1chr16:22203881-22203902TCCTTCCTCTCTTTCTTCTCC-6.28
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_00683chr16:22199332-22208185Adipose_Nuclei
SE_01979chr16:22200329-22204592Aorta
SE_10487chr16:22199321-22204649CD19_Primary
SE_11249chr16:22197627-22207934CD20
SE_11977chr16:22199271-22204610CD3
SE_14827chr16:22199054-22204871CD4_Memory_Primary_7pool
SE_15511chr16:22199096-22204729CD4_Memory_Primary_8pool
SE_16039chr16:22199414-22204303CD4_Naive_Primary_7pool
SE_16474chr16:22199243-22204501CD4_Naive_Primary_8pool
SE_16960chr16:22199331-22204777CD4p_CD225int_CD127p_Tmem
SE_17421chr16:22197856-22207948CD4p_CD25-_CD45RAp_Naive
SE_17990chr16:22197681-22205577CD4p_CD25-_CD45ROp_Memory
SE_20295chr16:22199376-22204902CD56
SE_21095chr16:22199644-22204726CD8_Memory_7pool
SE_21701chr16:22199330-22204547CD8_Naive_7pool
SE_22039chr16:22199259-22204858CD8_Naive_8pool
SE_22558chr16:22198010-22204854CD8_primiary
SE_27459chr16:22199727-22204779Esophagus
SE_29992chr16:22199834-22204871Fetal_Muscle
SE_42904chr16:22199330-22204886Lung
SE_48301chr16:22199834-22204912Psoas_Muscle
SE_49024chr16:22199991-22204825Right_Atrium
SE_51662chr16:22199489-22204834Skeletal_Muscle
SE_54110chr16:22199445-22204828Spleen
SE_61402chr16:22199511-22230924HBL1
SE_63046chr16:22199134-22211533Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr162220259622202946
Number: 1             
IDChromosomeStartEnd
GH16I022187chr162219893022205452
Enhancer Sequence
GTGTTTTGGC CCCGCCCCTG TCCTGTCCCG CCCCGCCCTC CGAAGTGGGC ACGCTCCTGC 60
TCCGCCCCCT GAATCCTGGC CACGTCCCTG GTCGGCCCAG ACGCGTAGCC CCGAGTCTCT 120
TTCCATGTTT TGACCACGCC CTTGACCCGC CCTTCAAATT GGGCACGCCT TCTTCCCCGC 180
TCACTGATTT CCTGGCCTAG CCCCTGAGCA GACCTCCAGA CCTAGCCCCG CCCCCGTTTT 240
ATAACCCCGC CCCTGCTTCA CGGCTTGGGC ACGCCTCTTC CCCGCCCCCT GACTTCAGAG 300
CCTAGTCCTG AGCCGCTCTC CAGGCCTAAC CCCGCCTTCA TGTCATAGCC ACGCCCCTTC 360
CCGCCCTTCC ATGTTTGGGC ACGCCTTCTG AGTCCTGGTC ACGCCTCTGT CCCGCCCCCT 420
GAATCTTTCC TACGTCCATG ACCCTCCCTC CAGGCCCTGG CCCTGCCCCT TTTTTCCTCC 480
CTCCGGCCTG TCCGGTTTCT GATATGGGCC AAGGCTCACA GCTTCCTCCG CCTTCTGGAC 540
CTTCTCCTAG TCCCTGCCCA GTCCCGGCCC ACCCCCAGAT TCTCCCTCAT TCTGGTTTCG 600
CCCCCTTTCT GGTCCTCCCC GCGCGCTTGA GCCCACCCTT TGGCTTCTCC TTTTGGGTCT 660
GTCCTTGCTC CTGCCTCTGG ACCCGGTCCC GCCCTTCTCG CGTGTAATTG AGTCCTGGCC 720
CCGCCCCCTC CCTCTCTGGC TTCACCCCTT TCCAGCTCCG CCTCCCGGGT AGGTTCTCCC 780
CGGAACCAGG CTGCCGCGTC GCTATGGGCT AACGCAGGCT CGGGTGACGT TGGTATGAGT 840
TTGCGCCGTC GGCTGCTGCT CTGTCTGGTA ACATTGCATT CGATCCACCC CGACCCAATG 900
TTCTGGGCTT CTCATTCACA CAGATCTGTG TGTTGACAGC CAGGGTTTGG GGAAAAACCG 960
AGACTCAAGC TTCTGCCGAG CCCGACTTGG CCTTTTTGGG TTCCTGTCTG AGGATGACAG 1020
CATAGTAAGC ACAGGTTTTA GTACCAGAAA GAGCATGAAA AATTTAAAAA AAAAAACTCT 1080
TAAAATAATT GGATGTCTCG ATGAAGTACC AATAAAGCTA TAATGGGAAA AATAGAGTTT 1140
AGTTGGTTAT ATTTTATGAT TTAGTACTGT TTCTATTTAT TAATTAGAGG TAGTGGTAAT 1200
CACCATAATC TTTAAAGTTT AAGGTCACGA AACTTCTTTA TCTAGCCCTG CTCTCCACAG 1260
AAACTTCGCC TCCTATCATC TTGGTATCAG TTATCAGTTG TAAGTACCAA GACATCAGTG 1320
TGTAAATACA ACCATGTATA GATCATAATA TGCACACGTG GGACTGGCAG AGAAGAAAAG 1380
CACCACAAGC CTGAGGTGGA TGGGATCGAA AGGGCTCATC AGAACCAACA TGGCCACCGC 1440
AGTGTGTGTC CCACTCTGCT GAACAAGGTG AGCAGTTTGG GAAGGAGCTA AAAAAAAATG 1500
TATGCTCCTC TCTGCTAGGC TGAATTTTAT GTGTGTATAT AATTTTTGAA AGAATAATAA 1560
TCCTATGTCT GTTTAATGCT TGACAGTGTA AAAGAGCTTT CATCTATGTG ATCTTATTTA 1620
ATTCTTACAG CTACTCTTAA ATAGGGTTTA TTACTCTCCT TTTATAGATG ACGAAAACTG 1680
GGGCTTTGTC TCATTCCAAA GAGCAGAGGA GGGTGGGGGT TTCTGCTCTA CAGCTGGGGG 1740
AATTTGGAGG AGCACCGCCT AAGCCGCCAC TGGCCTAAAC ACAACACGTG GTAACTTCTA 1800
CTCTTCTACA CTCTGGCCAT GCCAAGGCTT GCGGTTGAAC TCTGGTCTCG TTCTCTCAGA 1860
GCCGCAAACC TCGGACCATT TGAAGCTGGC GGTCCTGGGG CTTCCTTTCC TCTCGATAAC 1920
ATGTTTACAT CCAAACTCAC TTCCTTCCTC TCTTTCTTCT CCCTGCTAAT CCTGGGAAAT 1980
CTGTTCTTCG AGCAGGAAAA ACAATCTCAC ACTGCTCACG TTATTTTCTA GATCTTTTGA 2040
CTAGTGCCAA ACCTACTTTT GAAAATCCAA AAGCCAAGAA TCAATTTATT TGTTTTCTGG 2100
ATTTCTCCAA CTCATCTATT TCCTAACACT CTGGAAGCAG AATGTGTAAA 2150