EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS111-01857 
Organism
Homo sapiens 
Tissue/cell
KB 
Coordinate
chr16:22201200-22203470 
Target genes
Number: 7             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs145049847chr1622202002hg19
TF binding sites/motifs
Number: 22             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
E2F6MA0471.1chr16:22202295-22202306CCTTCCCGCCC-6.62
EWSR1-FLI1MA0149.1chr16:22201270-22201288GTAAGGAAGAAAGGAAGA+6.81
KLF13MA0657.1chr16:22201894-22201912TGGCCACGCCCCTATCTA+6.26
KLF14MA0740.1chr16:22202286-22202300AGCCACGCCCCTTC+6.1
KLF14MA0740.1chr16:22201895-22201909GGCCACGCCCCTAT+6.29
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
Klf12MA0742.1chr16:22201895-22201910GGCCACGCCCCTATC+6.39
SP1MA0079.4chr16:22202161-22202176CTAGCCCCGCCCCCG+6.13
SP1MA0079.4chr16:22201893-22201908CTGGCCACGCCCCTA+6.41
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
SP4MA0685.1chr16:22201893-22201910CTGGCCACGCCCCTATC+6.9
SP4MA0685.1chr16:22202654-22202671CTGGCCCCGCCCCCTCC+7.25
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
AATAGGGTGC GAATTCAGCG GGGCTGGAGG GGGCGACGCA AAGGCGGCAC CCTCCAATAA 60
AAATGAACAT GTAAGGAAGA AAGGAAGACC TCTCTAATGA GGGCATCGCA GGAGCAAGAC 120
GCTGCACTCG GGTCCTTTTA AATCACTATG TAATGGAGGG GAAATCCCTG CCCTCTCTTT 180
TCCCTTTCCG TAAACAACGA AGTAGAGGAT GTCCTCCTCC CACGAGGCCC GCCCTCGGAT 240
GCCCCGCCTG TCCCCGCAGG TGCGCAGCGT GGCCGTGACG CACACCTTCC AGATAGCCAA 300
GGCCCGCGCC CAGCTCGGCT ACGCGCCGGA TAAGTTTAGG TTCGCCGACG CCGTGGAGCT 360
ATACGTGCAG TCCACGACCC GGCGGCCCCG CGGCTCCACG GCGCGGACCC TCCTGCGCCT 420
GCTGCTCAGG CTGCTGCTGT TCCTCGGCTT GCTCGCCCTG GCCCTGCACT TCCTAGGCCT 480
GCAGCCTCTG CACGCCGCCG TGGAGCGCCT GTGACCGTCC GCCGTCCGCC GCCCGCTAGG 540
GTCGGCCCCG CTGCACCCTC GCCCACGCCC GGCTCCCTGG GCTTGTACCA GCCCCTGCCC 600
CGCCTTCTGG GTTTGAGCGC GCCTCCGCTC CGCCCCTTGA ATCCTGGTCA CGCCCCCGAG 660
CCGCTCTCCA GACCTAGCCC GGACCGCCGA CTTCTGGCCA CGCCCCTATC TACTCCCAGA 720
CCTTGCCTTG CGCCCTTCCT GTGTTTTGGC CCCGCCCCTG TCCTGTCCCG CCCCGCCCTC 780
CGAAGTGGGC ACGCTCCTGC TCCGCCCCCT GAATCCTGGC CACGTCCCTG GTCGGCCCAG 840
ACGCGTAGCC CCGAGTCTCT TTCCATGTTT TGACCACGCC CTTGACCCGC CCTTCAAATT 900
GGGCACGCCT TCTTCCCCGC TCACTGATTT CCTGGCCTAG CCCCTGAGCA GACCTCCAGA 960
CCTAGCCCCG CCCCCGTTTT ATAACCCCGC CCCTGCTTCA CGGCTTGGGC ACGCCTCTTC 1020
CCCGCCCCCT GACTTCAGAG CCTAGTCCTG AGCCGCTCTC CAGGCCTAAC CCCGCCTTCA 1080
TGTCATAGCC ACGCCCCTTC CCGCCCTTCC ATGTTTGGGC ACGCCTTCTG AGTCCTGGTC 1140
ACGCCTCTGT CCCGCCCCCT GAATCTTTCC TACGTCCATG ACCCTCCCTC CAGGCCCTGG 1200
CCCTGCCCCT TTTTTCCTCC CTCCGGCCTG TCCGGTTTCT GATATGGGCC AAGGCTCACA 1260
GCTTCCTCCG CCTTCTGGAC CTTCTCCTAG TCCCTGCCCA GTCCCGGCCC ACCCCCAGAT 1320
TCTCCCTCAT TCTGGTTTCG CCCCCTTTCT GGTCCTCCCC GCGCGCTTGA GCCCACCCTT 1380
TGGCTTCTCC TTTTGGGTCT GTCCTTGCTC CTGCCTCTGG ACCCGGTCCC GCCCTTCTCG 1440
CGTGTAATTG AGTCCTGGCC CCGCCCCCTC CCTCTCTGGC TTCACCCCTT TCCAGCTCCG 1500
CCTCCCGGGT AGGTTCTCCC CGGAACCAGG CTGCCGCGTC GCTATGGGCT AACGCAGGCT 1560
CGGGTGACGT TGGTATGAGT TTGCGCCGTC GGCTGCTGCT CTGTCTGGTA ACATTGCATT 1620
CGATCCACCC CGACCCAATG TTCTGGGCTT CTCATTCACA CAGATCTGTG TGTTGACAGC 1680
CAGGGTTTGG GGAAAAACCG AGACTCAAGC TTCTGCCGAG CCCGACTTGG CCTTTTTGGG 1740
TTCCTGTCTG AGGATGACAG CATAGTAAGC ACAGGTTTTA GTACCAGAAA GAGCATGAAA 1800
AATTTAAAAA AAAAAACTCT TAAAATAATT GGATGTCTCG ATGAAGTACC AATAAAGCTA 1860
TAATGGGAAA AATAGAGTTT AGTTGGTTAT ATTTTATGAT TTAGTACTGT TTCTATTTAT 1920
TAATTAGAGG TAGTGGTAAT CACCATAATC TTTAAAGTTT AAGGTCACGA AACTTCTTTA 1980
TCTAGCCCTG CTCTCCACAG AAACTTCGCC TCCTATCATC TTGGTATCAG TTATCAGTTG 2040
TAAGTACCAA GACATCAGTG TGTAAATACA ACCATGTATA GATCATAATA TGCACACGTG 2100
GGACTGGCAG AGAAGAAAAG CACCACAAGC CTGAGGTGGA TGGGATCGAA AGGGCTCATC 2160
AGAACCAACA TGGCCACCGC AGTGTGTGTC CCACTCTGCT GAACAAGGTG AGCAGTTTGG 2220
GAAGGAGCTA AAAAAAAATG TATGCTCCTC TCTGCTAGGC TGAATTTTAT 2270