EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS145-09015 
Organism
Homo sapiens 
Tissue/cell
NHBE 
Coordinate
chr16:22201220-22202960 
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
GGGCTGGAGG GGGCGACGCA AAGGCGGCAC CCTCCAATAA AAATGAACAT GTAAGGAAGA 60
AAGGAAGACC TCTCTAATGA GGGCATCGCA GGAGCAAGAC GCTGCACTCG GGTCCTTTTA 120
AATCACTATG TAATGGAGGG GAAATCCCTG CCCTCTCTTT TCCCTTTCCG TAAACAACGA 180
AGTAGAGGAT GTCCTCCTCC CACGAGGCCC GCCCTCGGAT GCCCCGCCTG TCCCCGCAGG 240
TGCGCAGCGT GGCCGTGACG CACACCTTCC AGATAGCCAA GGCCCGCGCC CAGCTCGGCT 300
ACGCGCCGGA TAAGTTTAGG TTCGCCGACG CCGTGGAGCT ATACGTGCAG TCCACGACCC 360
GGCGGCCCCG CGGCTCCACG GCGCGGACCC TCCTGCGCCT GCTGCTCAGG CTGCTGCTGT 420
TCCTCGGCTT GCTCGCCCTG GCCCTGCACT TCCTAGGCCT GCAGCCTCTG CACGCCGCCG 480
TGGAGCGCCT GTGACCGTCC GCCGTCCGCC GCCCGCTAGG GTCGGCCCCG CTGCACCCTC 540
GCCCACGCCC GGCTCCCTGG GCTTGTACCA GCCCCTGCCC CGCCTTCTGG GTTTGAGCGC 600
GCCTCCGCTC CGCCCCTTGA ATCCTGGTCA CGCCCCCGAG CCGCTCTCCA GACCTAGCCC 660
GGACCGCCGA CTTCTGGCCA CGCCCCTATC TACTCCCAGA CCTTGCCTTG CGCCCTTCCT 720
GTGTTTTGGC CCCGCCCCTG TCCTGTCCCG CCCCGCCCTC CGAAGTGGGC ACGCTCCTGC 780
TCCGCCCCCT GAATCCTGGC CACGTCCCTG GTCGGCCCAG ACGCGTAGCC CCGAGTCTCT 840
TTCCATGTTT TGACCACGCC CTTGACCCGC CCTTCAAATT GGGCACGCCT TCTTCCCCGC 900
TCACTGATTT CCTGGCCTAG CCCCTGAGCA GACCTCCAGA CCTAGCCCCG CCCCCGTTTT 960
ATAACCCCGC CCCTGCTTCA CGGCTTGGGC ACGCCTCTTC CCCGCCCCCT GACTTCAGAG 1020
CCTAGTCCTG AGCCGCTCTC CAGGCCTAAC CCCGCCTTCA TGTCATAGCC ACGCCCCTTC 1080
CCGCCCTTCC ATGTTTGGGC ACGCCTTCTG AGTCCTGGTC ACGCCTCTGT CCCGCCCCCT 1140
GAATCTTTCC TACGTCCATG ACCCTCCCTC CAGGCCCTGG CCCTGCCCCT TTTTTCCTCC 1200
CTCCGGCCTG TCCGGTTTCT GATATGGGCC AAGGCTCACA GCTTCCTCCG CCTTCTGGAC 1260
CTTCTCCTAG TCCCTGCCCA GTCCCGGCCC ACCCCCAGAT TCTCCCTCAT TCTGGTTTCG 1320
CCCCCTTTCT GGTCCTCCCC GCGCGCTTGA GCCCACCCTT TGGCTTCTCC TTTTGGGTCT 1380
GTCCTTGCTC CTGCCTCTGG ACCCGGTCCC GCCCTTCTCG CGTGTAATTG AGTCCTGGCC 1440
CCGCCCCCTC CCTCTCTGGC TTCACCCCTT TCCAGCTCCG CCTCCCGGGT AGGTTCTCCC 1500
CGGAACCAGG CTGCCGCGTC GCTATGGGCT AACGCAGGCT CGGGTGACGT TGGTATGAGT 1560
TTGCGCCGTC GGCTGCTGCT CTGTCTGGTA ACATTGCATT CGATCCACCC CGACCCAATG 1620
TTCTGGGCTT CTCATTCACA CAGATCTGTG TGTTGACAGC CAGGGTTTGG GGAAAAACCG 1680
AGACTCAAGC TTCTGCCGAG CCCGACTTGG CCTTTTTGGG TTCCTGTCTG AGGATGACAG 1740