EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS023-00413 
Organism
Homo sapiens 
Tissue/cell
CD8+ 
Coordinate
chr1:21655350-21657830 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs7543687chr121657507hg19
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HES2MA0616.2chr1:21656863-21656873GGCACGTGCC+6.02
HES2MA0616.2chr1:21656863-21656873GGCACGTGCC-6.02
KLF13MA0657.1chr1:21655872-21655890CAGAAAGGGGCGTGGCCT-8.83
KLF14MA0740.1chr1:21655875-21655889AAAGGGGCGTGGCC-7.28
Klf12MA0742.1chr1:21655874-21655889GAAAGGGGCGTGGCC-6.36
SP1MA0079.4chr1:21655876-21655891AAGGGGCGTGGCCTT-6.49
SP3MA0746.2chr1:21655876-21655889AAGGGGCGTGGCC-6.02
SP4MA0685.1chr1:21655874-21655891GAAAGGGGCGTGGCCTT-7.07
ZfxMA0146.2chr1:21657655-21657669GAGGCCGAGGCGGG-6.01
Number of super-enhancer constituents: 19             
IDCoordinateTissue/cell
SE_00105chr1:21656775-21671990Adipose_Nuclei
SE_00854chr1:21655127-21657780Adrenal_Gland
SE_01643chr1:21655308-21656605Aorta
SE_26127chr1:21655084-21657608Duodenum_Smooth_Muscle
SE_26770chr1:21655215-21657392Esophagus
SE_28486chr1:21654947-21657710Fetal_Intestine
SE_29337chr1:21654386-21657852Fetal_Intestine_Large
SE_31433chr1:21655247-21657689Gastric
SE_42174chr1:21655490-21656746Lung
SE_46660chr1:21657232-21657587Ovary
SE_47592chr1:21655381-21656725Pancreas
SE_47592chr1:21656951-21657495Pancreas
SE_50108chr1:21655247-21657708Sigmoid_Colon
SE_52633chr1:21655114-21657723Small_Intestine
SE_53334chr1:21655978-21656761Spleen
SE_56171chr1:21655842-21657532u87
SE_65263chr1:21655829-21657947Pancreatic_islets
SE_67931chr1:21655842-21657532u87
SE_68932chr1:21655176-21656735H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr12165680721657600
chr12165570421656517
chr12165726721657485
chr12165540021656713
Number: 1             
IDChromosomeStartEnd
GH01I021312chr12163897321657659
Enhancer Sequence
GGGTCTGCTT TCTAATCCCA GCTCTGCCAC CACAAGCTTT GGGCAAGGTA CCGCCTCTCT 60
GAGCCTCAGT TTCCTTATCC AATTGATCTA AAGGTGGAAT GGACATGCTG GCTGTTCATC 120
ATGACTGCTG CGAATCTCTC TCTAGACTCC CACCTCCCTT TGCATCCATT CCCCCTACCA 180
GGCGATGTTC TGATGGCTGA AGTGACCAAA TAAAATGCCC AGGATAGTGT TGGACCCAGA 240
GAAGACATGT AATAAATTAG ATTTCTAGCA TATTCTATGG TCCACCAGCA TCAGAATCAG 300
GCATTCTGCT GGAAATGTAG GTTCCTGGAC CCTCCCCCCG ACACTTACTG AGTTAGAACC 360
TCTAGGATGA GGGCAATGAA ACTTGCATTT GTAACCAGCA TTCCTGATGA TTCTCATGCA 420
CATGTCCGTT GAGAAGCACT GAAATCAATG CAACCTTATG CTTGCTACCG CCGACTTGCA 480
ATTCCTGGGT GTCCTGATTA CCAGCACAGA GGTGAGACTC ACCAGAAAGG GGCGTGGCCT 540
TCATAACCTG GTATTCTTCC TGATGGCTTA AAAACACGAG TACAGGCCTT GCAGTTAGAT 600
TGAGGTGCAA ATTCCAGTCC CTCTACTTAC TGGCTTAGCT GTGTGACCTT GGACACATGG 660
CTCAACCTCT GTGAGTCACC TTTCTCATGC TTAAAACGGC AGTAAATTAC CTCTACCTGC 720
CAGGGTTGTT GCAATGATCT GAGGAGGTGC CTTATGCAAA GCACAGTTCA TGTGCTCGGG 780
GCAAACAGTG GAAAAACAAA CCAGGAAATG CTTCTCTGTC TGTCTGTGCC TCCTACCTGC 840
CACAGGAGAA CTGAGGGTAG AATCTGTGTA CCCTTCTCAG CACACCACAA ATCCTAGTCA 900
CTTAGAGAGA CACAGACTGC CTACAAGGCT AGTCAACTCC CAACCACCTT TGCAGAAGGG 960
GGAGAGAGTG GGAGTTTGTG AAGAGCAAAA GCAGGAATTG GATGGGAAAA TGGTCTAGGG 1020
CTCACGTGGA GTGACCCAGG ACCCAGAGTC TCACCTCCCA AGGCTAGGCC TTGTAGGGCA 1080
GCAGGGCCAA GCATGCTGCA GGAAAGAACA CAGAGTCTGG AGCCAGACTG TTCAGGTTTA 1140
AATTTTGGCT CTGCTACTAC TAGCTTTGCC TGGCTGGCAA ACTCCTACCC ATCCTTCAAG 1200
ACCCAACTCA AACATCACCT CCCTGGACCA AGTTACTGGG CCTTTAAAGG CTCCTGCCCA 1260
CATACTCACT AAATACTTTT TTTTTTTTTT TTTTTTTTTT GAGACAGAGT CTCCCAGGTC 1320
CTATTCCTCT GGGCCTTTAA AGGCTCCTGC CCACATACTC GCCAAATACT TTTTTTTTTT 1380
TTTTTTTTTT TTTTTTGAGA CAGAGTCTCC CTCTGCCACC CAGGCTGGAG TGCAGTGGCA 1440
TGATCTCCAC TCACTGCAAC CTCTGCCTCC CGGGTTCAAG TGATTCTCAG CCTCCTGAGT 1500
AGCTGGGACC AAAGGCACGT GCCACCATGC CCAGCTAATT GTTTCGTATT TTTTGTAGAG 1560
ATGGGGTTTT GTCATGTTGC CCAGACTGGT CTCGAACTCC TGGCCTCAAG TGACCCACCC 1620
ATCGCAGCCT CCCAAAGTTC TGGGATTACA GGTGTGAGCT ACCGCCCCTA GCTGACCTCA 1680
CCAAATACTA TTCAGCAATT TACCTGCTAA TTTATCTATC TCTCCCACAG GCCTGGGAGC 1740
TCCTGGAAGG CACAGACACT GCCATGCCTG GCACAGGAAA CGTACTCAGC AAATGTTGCT 1800
TCAGTTTGAA TGCCAACTTT TTCAGCCTTC TGAGTTTCCT TTCTCTCCCC ATTAAATGCT 1860
TCCTAGGCTA ATCCTTCTTC CTCCCCCTGA CTCAGGTCCT TTCCTTTCTG GGTCTTAAAC 1920
TTCCACACCC CCTTCCTTGA AGGTCCCTAT CCGCTCACCC CTGAGCTGAT GCTGAACACA 1980
GGCTGTACAG GAAGACCTAA GATTAATTTC TTCCCTTTGC TGGCTGCAAA GGACTCTCAT 2040
GGAAGGTGAG GCACTCAGAG TCCATGAGAC TGGCTGATCA TAAGGACTAC GACCAGCTGG 2100
GTAGAAGTCA GTTATGGAGG AAGCACAAGT TGGATTCAGC CAGGGGTGGT GGTTCACGCC 2160
TGTCATCCCA AACTTTGGGG GTCCGAGGCA GGACGATCGC TTGAGCCCGA AGTTTGAGAC 2220
CAGCCTAGGC AACATAGCAA ACCCTGTCTC TACAAAAAAA TTAGGCCAGG CACGGTGGCT 2280
CATGCCTGTA ATCCCAGCAC TTTGGGAGGC CGAGGCGGGT GGATCACTTG AGGTCAGGAG 2340
ATCGAGACGA CCCTGGCCAA CATGGTGAAA CCCCATCTCT ACTAAAAATC CAAAAATTAG 2400
CCGGGCGTGG TGGTGCAGCG CCTGTAGTCC CAGCTACTCA GGAGGCTGAG GCAGAGGAAT 2460
CGCTTGAACC CAGGAGGTGA 2480