EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS012-13968 
Organism
Homo sapiens 
Tissue/cell
Caco-2 
Coordinate
chr16:22200840-22202980 
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
TGCTGATAGC TATCATTACT ACCCTTCAAA CCAGTGGGCC CCAAGCCATC TGGCAGCAGG 60
GGAAACACAG CTTAGACCCT GGAGAGCAAT CAGTTCTGCA TAATCGAATT CCTCTCTTAG 120
GGAAGCTTAG TTAATAAGCG AGGGCATGAA GGCTGCGACT GGGGCCCTCC TGGTCACAGT 180
TGGTCTGGGG TTGGGGGCAG GAAGCCAAGG TCGTTTCCTG CAGATGTTTC TGGCAGGCGT 240
TCACCTTCTC CTAGCGGATG CCTAAGAATG TATCAAGGGC CTCCTGAGTC CCAGCACCGT 300
GCTAGGCCGG GAAGATGAGT GTAGGGGTGA GACCTTTGCT TCTTAGGGAC CAAGGAGTTA 360
AATAGGGTGC GAATTCAGCG GGGCTGGAGG GGGCGACGCA AAGGCGGCAC CCTCCAATAA 420
AAATGAACAT GTAAGGAAGA AAGGAAGACC TCTCTAATGA GGGCATCGCA GGAGCAAGAC 480
GCTGCACTCG GGTCCTTTTA AATCACTATG TAATGGAGGG GAAATCCCTG CCCTCTCTTT 540
TCCCTTTCCG TAAACAACGA AGTAGAGGAT GTCCTCCTCC CACGAGGCCC GCCCTCGGAT 600
GCCCCGCCTG TCCCCGCAGG TGCGCAGCGT GGCCGTGACG CACACCTTCC AGATAGCCAA 660
GGCCCGCGCC CAGCTCGGCT ACGCGCCGGA TAAGTTTAGG TTCGCCGACG CCGTGGAGCT 720
ATACGTGCAG TCCACGACCC GGCGGCCCCG CGGCTCCACG GCGCGGACCC TCCTGCGCCT 780
GCTGCTCAGG CTGCTGCTGT TCCTCGGCTT GCTCGCCCTG GCCCTGCACT TCCTAGGCCT 840
GCAGCCTCTG CACGCCGCCG TGGAGCGCCT GTGACCGTCC GCCGTCCGCC GCCCGCTAGG 900
GTCGGCCCCG CTGCACCCTC GCCCACGCCC GGCTCCCTGG GCTTGTACCA GCCCCTGCCC 960
CGCCTTCTGG GTTTGAGCGC GCCTCCGCTC CGCCCCTTGA ATCCTGGTCA CGCCCCCGAG 1020
CCGCTCTCCA GACCTAGCCC GGACCGCCGA CTTCTGGCCA CGCCCCTATC TACTCCCAGA 1080
CCTTGCCTTG CGCCCTTCCT GTGTTTTGGC CCCGCCCCTG TCCTGTCCCG CCCCGCCCTC 1140
CGAAGTGGGC ACGCTCCTGC TCCGCCCCCT GAATCCTGGC CACGTCCCTG GTCGGCCCAG 1200
ACGCGTAGCC CCGAGTCTCT TTCCATGTTT TGACCACGCC CTTGACCCGC CCTTCAAATT 1260
GGGCACGCCT TCTTCCCCGC TCACTGATTT CCTGGCCTAG CCCCTGAGCA GACCTCCAGA 1320
CCTAGCCCCG CCCCCGTTTT ATAACCCCGC CCCTGCTTCA CGGCTTGGGC ACGCCTCTTC 1380
CCCGCCCCCT GACTTCAGAG CCTAGTCCTG AGCCGCTCTC CAGGCCTAAC CCCGCCTTCA 1440
TGTCATAGCC ACGCCCCTTC CCGCCCTTCC ATGTTTGGGC ACGCCTTCTG AGTCCTGGTC 1500
ACGCCTCTGT CCCGCCCCCT GAATCTTTCC TACGTCCATG ACCCTCCCTC CAGGCCCTGG 1560
CCCTGCCCCT TTTTTCCTCC CTCCGGCCTG TCCGGTTTCT GATATGGGCC AAGGCTCACA 1620
GCTTCCTCCG CCTTCTGGAC CTTCTCCTAG TCCCTGCCCA GTCCCGGCCC ACCCCCAGAT 1680
TCTCCCTCAT TCTGGTTTCG CCCCCTTTCT GGTCCTCCCC GCGCGCTTGA GCCCACCCTT 1740
TGGCTTCTCC TTTTGGGTCT GTCCTTGCTC CTGCCTCTGG ACCCGGTCCC GCCCTTCTCG 1800
CGTGTAATTG AGTCCTGGCC CCGCCCCCTC CCTCTCTGGC TTCACCCCTT TCCAGCTCCG 1860
CCTCCCGGGT AGGTTCTCCC CGGAACCAGG CTGCCGCGTC GCTATGGGCT AACGCAGGCT 1920
CGGGTGACGT TGGTATGAGT TTGCGCCGTC GGCTGCTGCT CTGTCTGGTA ACATTGCATT 1980
CGATCCACCC CGACCCAATG TTCTGGGCTT CTCATTCACA CAGATCTGTG TGTTGACAGC 2040
CAGGGTTTGG GGAAAAACCG AGACTCAAGC TTCTGCCGAG CCCGACTTGG CCTTTTTGGG 2100
TTCCTGTCTG AGGATGACAG CATAGTAAGC ACAGGTTTTA 2140