EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS078-06632 
Organism
Homo sapiens 
Tissue/cell
H2171 
Coordinate
chr16:22201400-22203300 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs145049847chr1622202002hg19
TF binding sites/motifs
Number: 21             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
E2F6MA0471.1chr16:22202295-22202306CCTTCCCGCCC-6.62
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
AGTAGAGGAT GTCCTCCTCC CACGAGGCCC GCCCTCGGAT GCCCCGCCTG TCCCCGCAGG 60
TGCGCAGCGT GGCCGTGACG CACACCTTCC AGATAGCCAA GGCCCGCGCC CAGCTCGGCT 120
ACGCGCCGGA TAAGTTTAGG TTCGCCGACG CCGTGGAGCT ATACGTGCAG TCCACGACCC 180
GGCGGCCCCG CGGCTCCACG GCGCGGACCC TCCTGCGCCT GCTGCTCAGG CTGCTGCTGT 240
TCCTCGGCTT GCTCGCCCTG GCCCTGCACT TCCTAGGCCT GCAGCCTCTG CACGCCGCCG 300
TGGAGCGCCT GTGACCGTCC GCCGTCCGCC GCCCGCTAGG GTCGGCCCCG CTGCACCCTC 360
GCCCACGCCC GGCTCCCTGG GCTTGTACCA GCCCCTGCCC CGCCTTCTGG GTTTGAGCGC 420
GCCTCCGCTC CGCCCCTTGA ATCCTGGTCA CGCCCCCGAG CCGCTCTCCA GACCTAGCCC 480
GGACCGCCGA CTTCTGGCCA CGCCCCTATC TACTCCCAGA CCTTGCCTTG CGCCCTTCCT 540
GTGTTTTGGC CCCGCCCCTG TCCTGTCCCG CCCCGCCCTC CGAAGTGGGC ACGCTCCTGC 600
TCCGCCCCCT GAATCCTGGC CACGTCCCTG GTCGGCCCAG ACGCGTAGCC CCGAGTCTCT 660
TTCCATGTTT TGACCACGCC CTTGACCCGC CCTTCAAATT GGGCACGCCT TCTTCCCCGC 720
TCACTGATTT CCTGGCCTAG CCCCTGAGCA GACCTCCAGA CCTAGCCCCG CCCCCGTTTT 780
ATAACCCCGC CCCTGCTTCA CGGCTTGGGC ACGCCTCTTC CCCGCCCCCT GACTTCAGAG 840
CCTAGTCCTG AGCCGCTCTC CAGGCCTAAC CCCGCCTTCA TGTCATAGCC ACGCCCCTTC 900
CCGCCCTTCC ATGTTTGGGC ACGCCTTCTG AGTCCTGGTC ACGCCTCTGT CCCGCCCCCT 960
GAATCTTTCC TACGTCCATG ACCCTCCCTC CAGGCCCTGG CCCTGCCCCT TTTTTCCTCC 1020
CTCCGGCCTG TCCGGTTTCT GATATGGGCC AAGGCTCACA GCTTCCTCCG CCTTCTGGAC 1080
CTTCTCCTAG TCCCTGCCCA GTCCCGGCCC ACCCCCAGAT TCTCCCTCAT TCTGGTTTCG 1140
CCCCCTTTCT GGTCCTCCCC GCGCGCTTGA GCCCACCCTT TGGCTTCTCC TTTTGGGTCT 1200
GTCCTTGCTC CTGCCTCTGG ACCCGGTCCC GCCCTTCTCG CGTGTAATTG AGTCCTGGCC 1260
CCGCCCCCTC CCTCTCTGGC TTCACCCCTT TCCAGCTCCG CCTCCCGGGT AGGTTCTCCC 1320
CGGAACCAGG CTGCCGCGTC GCTATGGGCT AACGCAGGCT CGGGTGACGT TGGTATGAGT 1380
TTGCGCCGTC GGCTGCTGCT CTGTCTGGTA ACATTGCATT CGATCCACCC CGACCCAATG 1440
TTCTGGGCTT CTCATTCACA CAGATCTGTG TGTTGACAGC CAGGGTTTGG GGAAAAACCG 1500
AGACTCAAGC TTCTGCCGAG CCCGACTTGG CCTTTTTGGG TTCCTGTCTG AGGATGACAG 1560
CATAGTAAGC ACAGGTTTTA GTACCAGAAA GAGCATGAAA AATTTAAAAA AAAAAACTCT 1620
TAAAATAATT GGATGTCTCG ATGAAGTACC AATAAAGCTA TAATGGGAAA AATAGAGTTT 1680
AGTTGGTTAT ATTTTATGAT TTAGTACTGT TTCTATTTAT TAATTAGAGG TAGTGGTAAT 1740
CACCATAATC TTTAAAGTTT AAGGTCACGA AACTTCTTTA TCTAGCCCTG CTCTCCACAG 1800
AAACTTCGCC TCCTATCATC TTGGTATCAG TTATCAGTTG TAAGTACCAA GACATCAGTG 1860
TGTAAATACA ACCATGTATA GATCATAATA TGCACACGTG 1900