EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS184-12214 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr16:22201230-22203000 
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
GGGCGACGCA AAGGCGGCAC CCTCCAATAA AAATGAACAT GTAAGGAAGA AAGGAAGACC 60
TCTCTAATGA GGGCATCGCA GGAGCAAGAC GCTGCACTCG GGTCCTTTTA AATCACTATG 120
TAATGGAGGG GAAATCCCTG CCCTCTCTTT TCCCTTTCCG TAAACAACGA AGTAGAGGAT 180
GTCCTCCTCC CACGAGGCCC GCCCTCGGAT GCCCCGCCTG TCCCCGCAGG TGCGCAGCGT 240
GGCCGTGACG CACACCTTCC AGATAGCCAA GGCCCGCGCC CAGCTCGGCT ACGCGCCGGA 300
TAAGTTTAGG TTCGCCGACG CCGTGGAGCT ATACGTGCAG TCCACGACCC GGCGGCCCCG 360
CGGCTCCACG GCGCGGACCC TCCTGCGCCT GCTGCTCAGG CTGCTGCTGT TCCTCGGCTT 420
GCTCGCCCTG GCCCTGCACT TCCTAGGCCT GCAGCCTCTG CACGCCGCCG TGGAGCGCCT 480
GTGACCGTCC GCCGTCCGCC GCCCGCTAGG GTCGGCCCCG CTGCACCCTC GCCCACGCCC 540
GGCTCCCTGG GCTTGTACCA GCCCCTGCCC CGCCTTCTGG GTTTGAGCGC GCCTCCGCTC 600
CGCCCCTTGA ATCCTGGTCA CGCCCCCGAG CCGCTCTCCA GACCTAGCCC GGACCGCCGA 660
CTTCTGGCCA CGCCCCTATC TACTCCCAGA CCTTGCCTTG CGCCCTTCCT GTGTTTTGGC 720
CCCGCCCCTG TCCTGTCCCG CCCCGCCCTC CGAAGTGGGC ACGCTCCTGC TCCGCCCCCT 780
GAATCCTGGC CACGTCCCTG GTCGGCCCAG ACGCGTAGCC CCGAGTCTCT TTCCATGTTT 840
TGACCACGCC CTTGACCCGC CCTTCAAATT GGGCACGCCT TCTTCCCCGC TCACTGATTT 900
CCTGGCCTAG CCCCTGAGCA GACCTCCAGA CCTAGCCCCG CCCCCGTTTT ATAACCCCGC 960
CCCTGCTTCA CGGCTTGGGC ACGCCTCTTC CCCGCCCCCT GACTTCAGAG CCTAGTCCTG 1020
AGCCGCTCTC CAGGCCTAAC CCCGCCTTCA TGTCATAGCC ACGCCCCTTC CCGCCCTTCC 1080
ATGTTTGGGC ACGCCTTCTG AGTCCTGGTC ACGCCTCTGT CCCGCCCCCT GAATCTTTCC 1140
TACGTCCATG ACCCTCCCTC CAGGCCCTGG CCCTGCCCCT TTTTTCCTCC CTCCGGCCTG 1200
TCCGGTTTCT GATATGGGCC AAGGCTCACA GCTTCCTCCG CCTTCTGGAC CTTCTCCTAG 1260
TCCCTGCCCA GTCCCGGCCC ACCCCCAGAT TCTCCCTCAT TCTGGTTTCG CCCCCTTTCT 1320
GGTCCTCCCC GCGCGCTTGA GCCCACCCTT TGGCTTCTCC TTTTGGGTCT GTCCTTGCTC 1380
CTGCCTCTGG ACCCGGTCCC GCCCTTCTCG CGTGTAATTG AGTCCTGGCC CCGCCCCCTC 1440
CCTCTCTGGC TTCACCCCTT TCCAGCTCCG CCTCCCGGGT AGGTTCTCCC CGGAACCAGG 1500
CTGCCGCGTC GCTATGGGCT AACGCAGGCT CGGGTGACGT TGGTATGAGT TTGCGCCGTC 1560
GGCTGCTGCT CTGTCTGGTA ACATTGCATT CGATCCACCC CGACCCAATG TTCTGGGCTT 1620
CTCATTCACA CAGATCTGTG TGTTGACAGC CAGGGTTTGG GGAAAAACCG AGACTCAAGC 1680
TTCTGCCGAG CCCGACTTGG CCTTTTTGGG TTCCTGTCTG AGGATGACAG CATAGTAAGC 1740
ACAGGTTTTA GTACCAGAAA GAGCATGAAA 1770