EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS034-11070 
Organism
Homo sapiens 
Tissue/cell
ECC-1 
Coordinate
chr16:22200930-22203030 
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
CAGTTCTGCA TAATCGAATT CCTCTCTTAG GGAAGCTTAG TTAATAAGCG AGGGCATGAA 60
GGCTGCGACT GGGGCCCTCC TGGTCACAGT TGGTCTGGGG TTGGGGGCAG GAAGCCAAGG 120
TCGTTTCCTG CAGATGTTTC TGGCAGGCGT TCACCTTCTC CTAGCGGATG CCTAAGAATG 180
TATCAAGGGC CTCCTGAGTC CCAGCACCGT GCTAGGCCGG GAAGATGAGT GTAGGGGTGA 240
GACCTTTGCT TCTTAGGGAC CAAGGAGTTA AATAGGGTGC GAATTCAGCG GGGCTGGAGG 300
GGGCGACGCA AAGGCGGCAC CCTCCAATAA AAATGAACAT GTAAGGAAGA AAGGAAGACC 360
TCTCTAATGA GGGCATCGCA GGAGCAAGAC GCTGCACTCG GGTCCTTTTA AATCACTATG 420
TAATGGAGGG GAAATCCCTG CCCTCTCTTT TCCCTTTCCG TAAACAACGA AGTAGAGGAT 480
GTCCTCCTCC CACGAGGCCC GCCCTCGGAT GCCCCGCCTG TCCCCGCAGG TGCGCAGCGT 540
GGCCGTGACG CACACCTTCC AGATAGCCAA GGCCCGCGCC CAGCTCGGCT ACGCGCCGGA 600
TAAGTTTAGG TTCGCCGACG CCGTGGAGCT ATACGTGCAG TCCACGACCC GGCGGCCCCG 660
CGGCTCCACG GCGCGGACCC TCCTGCGCCT GCTGCTCAGG CTGCTGCTGT TCCTCGGCTT 720
GCTCGCCCTG GCCCTGCACT TCCTAGGCCT GCAGCCTCTG CACGCCGCCG TGGAGCGCCT 780
GTGACCGTCC GCCGTCCGCC GCCCGCTAGG GTCGGCCCCG CTGCACCCTC GCCCACGCCC 840
GGCTCCCTGG GCTTGTACCA GCCCCTGCCC CGCCTTCTGG GTTTGAGCGC GCCTCCGCTC 900
CGCCCCTTGA ATCCTGGTCA CGCCCCCGAG CCGCTCTCCA GACCTAGCCC GGACCGCCGA 960
CTTCTGGCCA CGCCCCTATC TACTCCCAGA CCTTGCCTTG CGCCCTTCCT GTGTTTTGGC 1020
CCCGCCCCTG TCCTGTCCCG CCCCGCCCTC CGAAGTGGGC ACGCTCCTGC TCCGCCCCCT 1080
GAATCCTGGC CACGTCCCTG GTCGGCCCAG ACGCGTAGCC CCGAGTCTCT TTCCATGTTT 1140
TGACCACGCC CTTGACCCGC CCTTCAAATT GGGCACGCCT TCTTCCCCGC TCACTGATTT 1200
CCTGGCCTAG CCCCTGAGCA GACCTCCAGA CCTAGCCCCG CCCCCGTTTT ATAACCCCGC 1260
CCCTGCTTCA CGGCTTGGGC ACGCCTCTTC CCCGCCCCCT GACTTCAGAG CCTAGTCCTG 1320
AGCCGCTCTC CAGGCCTAAC CCCGCCTTCA TGTCATAGCC ACGCCCCTTC CCGCCCTTCC 1380
ATGTTTGGGC ACGCCTTCTG AGTCCTGGTC ACGCCTCTGT CCCGCCCCCT GAATCTTTCC 1440
TACGTCCATG ACCCTCCCTC CAGGCCCTGG CCCTGCCCCT TTTTTCCTCC CTCCGGCCTG 1500
TCCGGTTTCT GATATGGGCC AAGGCTCACA GCTTCCTCCG CCTTCTGGAC CTTCTCCTAG 1560
TCCCTGCCCA GTCCCGGCCC ACCCCCAGAT TCTCCCTCAT TCTGGTTTCG CCCCCTTTCT 1620
GGTCCTCCCC GCGCGCTTGA GCCCACCCTT TGGCTTCTCC TTTTGGGTCT GTCCTTGCTC 1680
CTGCCTCTGG ACCCGGTCCC GCCCTTCTCG CGTGTAATTG AGTCCTGGCC CCGCCCCCTC 1740
CCTCTCTGGC TTCACCCCTT TCCAGCTCCG CCTCCCGGGT AGGTTCTCCC CGGAACCAGG 1800
CTGCCGCGTC GCTATGGGCT AACGCAGGCT CGGGTGACGT TGGTATGAGT TTGCGCCGTC 1860
GGCTGCTGCT CTGTCTGGTA ACATTGCATT CGATCCACCC CGACCCAATG TTCTGGGCTT 1920
CTCATTCACA CAGATCTGTG TGTTGACAGC CAGGGTTTGG GGAAAAACCG AGACTCAAGC 1980
TTCTGCCGAG CCCGACTTGG CCTTTTTGGG TTCCTGTCTG AGGATGACAG CATAGTAAGC 2040
ACAGGTTTTA GTACCAGAAA GAGCATGAAA AATTTAAAAA AAAAAACTCT TAAAATAATT 2100