EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS118-00237 
Organism
Homo sapiens 
Tissue/cell
Liver 
Coordinate
chr1:21655160-21657780 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs7543687chr121657507hg19
TF binding sites/motifs
Number: 10             
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
ZfxMA0146.2chr1:21655333-21655347CAGGCCTCGGCTGC-6.6
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
CAGAAGAATC GCTTGAACCT GGGAGATGGA GGTTGCAGTG AGTTGAGGTC ACTCCACTGT 60
ACTCCAGCCT GAGCAACAAG AGCGAACCTC CATCTCGAAA AAAAAAAAAA AAAAAAAAAG 120
AATCTCTGTG TGGAAGTCTG CAAAAGCAAC CACGTTGGGT ATTAGGAGGA ACACAGGCCT 180
CGGCTGCTGA GGGTCTGCTT TCTAATCCCA GCTCTGCCAC CACAAGCTTT GGGCAAGGTA 240
CCGCCTCTCT GAGCCTCAGT TTCCTTATCC AATTGATCTA AAGGTGGAAT GGACATGCTG 300
GCTGTTCATC ATGACTGCTG CGAATCTCTC TCTAGACTCC CACCTCCCTT TGCATCCATT 360
CCCCCTACCA GGCGATGTTC TGATGGCTGA AGTGACCAAA TAAAATGCCC AGGATAGTGT 420
TGGACCCAGA GAAGACATGT AATAAATTAG ATTTCTAGCA TATTCTATGG TCCACCAGCA 480
TCAGAATCAG GCATTCTGCT GGAAATGTAG GTTCCTGGAC CCTCCCCCCG ACACTTACTG 540
AGTTAGAACC TCTAGGATGA GGGCAATGAA ACTTGCATTT GTAACCAGCA TTCCTGATGA 600
TTCTCATGCA CATGTCCGTT GAGAAGCACT GAAATCAATG CAACCTTATG CTTGCTACCG 660
CCGACTTGCA ATTCCTGGGT GTCCTGATTA CCAGCACAGA GGTGAGACTC ACCAGAAAGG 720
GGCGTGGCCT TCATAACCTG GTATTCTTCC TGATGGCTTA AAAACACGAG TACAGGCCTT 780
GCAGTTAGAT TGAGGTGCAA ATTCCAGTCC CTCTACTTAC TGGCTTAGCT GTGTGACCTT 840
GGACACATGG CTCAACCTCT GTGAGTCACC TTTCTCATGC TTAAAACGGC AGTAAATTAC 900
CTCTACCTGC CAGGGTTGTT GCAATGATCT GAGGAGGTGC CTTATGCAAA GCACAGTTCA 960
TGTGCTCGGG GCAAACAGTG GAAAAACAAA CCAGGAAATG CTTCTCTGTC TGTCTGTGCC 1020
TCCTACCTGC CACAGGAGAA CTGAGGGTAG AATCTGTGTA CCCTTCTCAG CACACCACAA 1080
ATCCTAGTCA CTTAGAGAGA CACAGACTGC CTACAAGGCT AGTCAACTCC CAACCACCTT 1140
TGCAGAAGGG GGAGAGAGTG GGAGTTTGTG AAGAGCAAAA GCAGGAATTG GATGGGAAAA 1200
TGGTCTAGGG CTCACGTGGA GTGACCCAGG ACCCAGAGTC TCACCTCCCA AGGCTAGGCC 1260
TTGTAGGGCA GCAGGGCCAA GCATGCTGCA GGAAAGAACA CAGAGTCTGG AGCCAGACTG 1320
TTCAGGTTTA AATTTTGGCT CTGCTACTAC TAGCTTTGCC TGGCTGGCAA ACTCCTACCC 1380
ATCCTTCAAG ACCCAACTCA AACATCACCT CCCTGGACCA AGTTACTGGG CCTTTAAAGG 1440
CTCCTGCCCA CATACTCACT AAATACTTTT TTTTTTTTTT TTTTTTTTTT GAGACAGAGT 1500
CTCCCAGGTC CTATTCCTCT GGGCCTTTAA AGGCTCCTGC CCACATACTC GCCAAATACT 1560
TTTTTTTTTT TTTTTTTTTT TTTTTTGAGA CAGAGTCTCC CTCTGCCACC CAGGCTGGAG 1620
TGCAGTGGCA TGATCTCCAC TCACTGCAAC CTCTGCCTCC CGGGTTCAAG TGATTCTCAG 1680
CCTCCTGAGT AGCTGGGACC AAAGGCACGT GCCACCATGC CCAGCTAATT GTTTCGTATT 1740
TTTTGTAGAG ATGGGGTTTT GTCATGTTGC CCAGACTGGT CTCGAACTCC TGGCCTCAAG 1800
TGACCCACCC ATCGCAGCCT CCCAAAGTTC TGGGATTACA GGTGTGAGCT ACCGCCCCTA 1860
GCTGACCTCA CCAAATACTA TTCAGCAATT TACCTGCTAA TTTATCTATC TCTCCCACAG 1920
GCCTGGGAGC TCCTGGAAGG CACAGACACT GCCATGCCTG GCACAGGAAA CGTACTCAGC 1980
AAATGTTGCT TCAGTTTGAA TGCCAACTTT TTCAGCCTTC TGAGTTTCCT TTCTCTCCCC 2040
ATTAAATGCT TCCTAGGCTA ATCCTTCTTC CTCCCCCTGA CTCAGGTCCT TTCCTTTCTG 2100
GGTCTTAAAC TTCCACACCC CCTTCCTTGA AGGTCCCTAT CCGCTCACCC CTGAGCTGAT 2160
GCTGAACACA GGCTGTACAG GAAGACCTAA GATTAATTTC TTCCCTTTGC TGGCTGCAAA 2220
GGACTCTCAT GGAAGGTGAG GCACTCAGAG TCCATGAGAC TGGCTGATCA TAAGGACTAC 2280
GACCAGCTGG GTAGAAGTCA GTTATGGAGG AAGCACAAGT TGGATTCAGC CAGGGGTGGT 2340
GGTTCACGCC TGTCATCCCA AACTTTGGGG GTCCGAGGCA GGACGATCGC TTGAGCCCGA 2400
AGTTTGAGAC CAGCCTAGGC AACATAGCAA ACCCTGTCTC TACAAAAAAA TTAGGCCAGG 2460
CACGGTGGCT CATGCCTGTA ATCCCAGCAC TTTGGGAGGC CGAGGCGGGT GGATCACTTG 2520
AGGTCAGGAG ATCGAGACGA CCCTGGCCAA CATGGTGAAA CCCCATCTCT ACTAAAAATC 2580
CAAAAATTAG CCGGGCGTGG TGGTGCAGCG CCTGTAGTCC 2620