EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS196-10811 
Organism
Homo sapiens 
Tissue/cell
ZR75-1 
Coordinate
chr16:22201000-22203450 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs145049847chr1622202002hg19
TF binding sites/motifs
Number: 23             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
DMRT3MA0610.1chr16:22201106-22201117AATGTATCAAG+6.02
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: 2             
ChromosomeStartEnd
chr162220117022202123
chr162220259622202946
Number: 1             
IDChromosomeStartEnd
GH16I022187chr162219893022205452
Enhancer Sequence
GGGGCCCTCC TGGTCACAGT TGGTCTGGGG TTGGGGGCAG GAAGCCAAGG TCGTTTCCTG 60
CAGATGTTTC TGGCAGGCGT TCACCTTCTC CTAGCGGATG CCTAAGAATG TATCAAGGGC 120
CTCCTGAGTC CCAGCACCGT GCTAGGCCGG GAAGATGAGT GTAGGGGTGA GACCTTTGCT 180
TCTTAGGGAC CAAGGAGTTA AATAGGGTGC GAATTCAGCG GGGCTGGAGG GGGCGACGCA 240
AAGGCGGCAC CCTCCAATAA AAATGAACAT GTAAGGAAGA AAGGAAGACC TCTCTAATGA 300
GGGCATCGCA GGAGCAAGAC GCTGCACTCG GGTCCTTTTA AATCACTATG TAATGGAGGG 360
GAAATCCCTG CCCTCTCTTT TCCCTTTCCG TAAACAACGA AGTAGAGGAT GTCCTCCTCC 420
CACGAGGCCC GCCCTCGGAT GCCCCGCCTG TCCCCGCAGG TGCGCAGCGT GGCCGTGACG 480
CACACCTTCC AGATAGCCAA GGCCCGCGCC CAGCTCGGCT ACGCGCCGGA TAAGTTTAGG 540
TTCGCCGACG CCGTGGAGCT ATACGTGCAG TCCACGACCC GGCGGCCCCG CGGCTCCACG 600
GCGCGGACCC TCCTGCGCCT GCTGCTCAGG CTGCTGCTGT TCCTCGGCTT GCTCGCCCTG 660
GCCCTGCACT TCCTAGGCCT GCAGCCTCTG CACGCCGCCG TGGAGCGCCT GTGACCGTCC 720
GCCGTCCGCC GCCCGCTAGG GTCGGCCCCG CTGCACCCTC GCCCACGCCC GGCTCCCTGG 780
GCTTGTACCA GCCCCTGCCC CGCCTTCTGG GTTTGAGCGC GCCTCCGCTC CGCCCCTTGA 840
ATCCTGGTCA CGCCCCCGAG CCGCTCTCCA GACCTAGCCC GGACCGCCGA CTTCTGGCCA 900
CGCCCCTATC TACTCCCAGA CCTTGCCTTG CGCCCTTCCT GTGTTTTGGC CCCGCCCCTG 960
TCCTGTCCCG CCCCGCCCTC CGAAGTGGGC ACGCTCCTGC TCCGCCCCCT GAATCCTGGC 1020
CACGTCCCTG GTCGGCCCAG ACGCGTAGCC CCGAGTCTCT TTCCATGTTT TGACCACGCC 1080
CTTGACCCGC CCTTCAAATT GGGCACGCCT TCTTCCCCGC TCACTGATTT CCTGGCCTAG 1140
CCCCTGAGCA GACCTCCAGA CCTAGCCCCG CCCCCGTTTT ATAACCCCGC CCCTGCTTCA 1200
CGGCTTGGGC ACGCCTCTTC CCCGCCCCCT GACTTCAGAG CCTAGTCCTG AGCCGCTCTC 1260
CAGGCCTAAC CCCGCCTTCA TGTCATAGCC ACGCCCCTTC CCGCCCTTCC ATGTTTGGGC 1320
ACGCCTTCTG AGTCCTGGTC ACGCCTCTGT CCCGCCCCCT GAATCTTTCC TACGTCCATG 1380
ACCCTCCCTC CAGGCCCTGG CCCTGCCCCT TTTTTCCTCC CTCCGGCCTG TCCGGTTTCT 1440
GATATGGGCC AAGGCTCACA GCTTCCTCCG CCTTCTGGAC CTTCTCCTAG TCCCTGCCCA 1500
GTCCCGGCCC ACCCCCAGAT TCTCCCTCAT TCTGGTTTCG CCCCCTTTCT GGTCCTCCCC 1560
GCGCGCTTGA GCCCACCCTT TGGCTTCTCC TTTTGGGTCT GTCCTTGCTC CTGCCTCTGG 1620
ACCCGGTCCC GCCCTTCTCG CGTGTAATTG AGTCCTGGCC CCGCCCCCTC CCTCTCTGGC 1680
TTCACCCCTT TCCAGCTCCG CCTCCCGGGT AGGTTCTCCC CGGAACCAGG CTGCCGCGTC 1740
GCTATGGGCT AACGCAGGCT CGGGTGACGT TGGTATGAGT TTGCGCCGTC GGCTGCTGCT 1800
CTGTCTGGTA ACATTGCATT CGATCCACCC CGACCCAATG TTCTGGGCTT CTCATTCACA 1860
CAGATCTGTG TGTTGACAGC CAGGGTTTGG GGAAAAACCG AGACTCAAGC TTCTGCCGAG 1920
CCCGACTTGG CCTTTTTGGG TTCCTGTCTG AGGATGACAG CATAGTAAGC ACAGGTTTTA 1980
GTACCAGAAA GAGCATGAAA AATTTAAAAA AAAAAACTCT TAAAATAATT GGATGTCTCG 2040
ATGAAGTACC AATAAAGCTA TAATGGGAAA AATAGAGTTT AGTTGGTTAT ATTTTATGAT 2100
TTAGTACTGT TTCTATTTAT TAATTAGAGG TAGTGGTAAT CACCATAATC TTTAAAGTTT 2160
AAGGTCACGA AACTTCTTTA TCTAGCCCTG CTCTCCACAG AAACTTCGCC TCCTATCATC 2220
TTGGTATCAG TTATCAGTTG TAAGTACCAA GACATCAGTG TGTAAATACA ACCATGTATA 2280
GATCATAATA TGCACACGTG GGACTGGCAG AGAAGAAAAG CACCACAAGC CTGAGGTGGA 2340
TGGGATCGAA AGGGCTCATC AGAACCAACA TGGCCACCGC AGTGTGTGTC CCACTCTGCT 2400
GAACAAGGTG AGCAGTTTGG GAAGGAGCTA AAAAAAAATG TATGCTCCTC 2450