EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS056-00231 
Organism
Homo sapiens 
Tissue/cell
GC_B_cell 
Coordinate
chr1:21655400-21657930 
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
CCGCCTCTCT GAGCCTCAGT TTCCTTATCC AATTGATCTA AAGGTGGAAT GGACATGCTG 60
GCTGTTCATC ATGACTGCTG CGAATCTCTC TCTAGACTCC CACCTCCCTT TGCATCCATT 120
CCCCCTACCA GGCGATGTTC TGATGGCTGA AGTGACCAAA TAAAATGCCC AGGATAGTGT 180
TGGACCCAGA GAAGACATGT AATAAATTAG ATTTCTAGCA TATTCTATGG TCCACCAGCA 240
TCAGAATCAG GCATTCTGCT GGAAATGTAG GTTCCTGGAC CCTCCCCCCG ACACTTACTG 300
AGTTAGAACC TCTAGGATGA GGGCAATGAA ACTTGCATTT GTAACCAGCA TTCCTGATGA 360
TTCTCATGCA CATGTCCGTT GAGAAGCACT GAAATCAATG CAACCTTATG CTTGCTACCG 420
CCGACTTGCA ATTCCTGGGT GTCCTGATTA CCAGCACAGA GGTGAGACTC ACCAGAAAGG 480
GGCGTGGCCT TCATAACCTG GTATTCTTCC TGATGGCTTA AAAACACGAG TACAGGCCTT 540
GCAGTTAGAT TGAGGTGCAA ATTCCAGTCC CTCTACTTAC TGGCTTAGCT GTGTGACCTT 600
GGACACATGG CTCAACCTCT GTGAGTCACC TTTCTCATGC TTAAAACGGC AGTAAATTAC 660
CTCTACCTGC CAGGGTTGTT GCAATGATCT GAGGAGGTGC CTTATGCAAA GCACAGTTCA 720
TGTGCTCGGG GCAAACAGTG GAAAAACAAA CCAGGAAATG CTTCTCTGTC TGTCTGTGCC 780
TCCTACCTGC CACAGGAGAA CTGAGGGTAG AATCTGTGTA CCCTTCTCAG CACACCACAA 840
ATCCTAGTCA CTTAGAGAGA CACAGACTGC CTACAAGGCT AGTCAACTCC CAACCACCTT 900
TGCAGAAGGG GGAGAGAGTG GGAGTTTGTG AAGAGCAAAA GCAGGAATTG GATGGGAAAA 960
TGGTCTAGGG CTCACGTGGA GTGACCCAGG ACCCAGAGTC TCACCTCCCA AGGCTAGGCC 1020
TTGTAGGGCA GCAGGGCCAA GCATGCTGCA GGAAAGAACA CAGAGTCTGG AGCCAGACTG 1080
TTCAGGTTTA AATTTTGGCT CTGCTACTAC TAGCTTTGCC TGGCTGGCAA ACTCCTACCC 1140
ATCCTTCAAG ACCCAACTCA AACATCACCT CCCTGGACCA AGTTACTGGG CCTTTAAAGG 1200
CTCCTGCCCA CATACTCACT AAATACTTTT TTTTTTTTTT TTTTTTTTTT GAGACAGAGT 1260
CTCCCAGGTC CTATTCCTCT GGGCCTTTAA AGGCTCCTGC CCACATACTC GCCAAATACT 1320
TTTTTTTTTT TTTTTTTTTT TTTTTTGAGA CAGAGTCTCC CTCTGCCACC CAGGCTGGAG 1380
TGCAGTGGCA TGATCTCCAC TCACTGCAAC CTCTGCCTCC CGGGTTCAAG TGATTCTCAG 1440
CCTCCTGAGT AGCTGGGACC AAAGGCACGT GCCACCATGC CCAGCTAATT GTTTCGTATT 1500
TTTTGTAGAG ATGGGGTTTT GTCATGTTGC CCAGACTGGT CTCGAACTCC TGGCCTCAAG 1560
TGACCCACCC ATCGCAGCCT CCCAAAGTTC TGGGATTACA GGTGTGAGCT ACCGCCCCTA 1620
GCTGACCTCA CCAAATACTA TTCAGCAATT TACCTGCTAA TTTATCTATC TCTCCCACAG 1680
GCCTGGGAGC TCCTGGAAGG CACAGACACT GCCATGCCTG GCACAGGAAA CGTACTCAGC 1740
AAATGTTGCT TCAGTTTGAA TGCCAACTTT TTCAGCCTTC TGAGTTTCCT TTCTCTCCCC 1800
ATTAAATGCT TCCTAGGCTA ATCCTTCTTC CTCCCCCTGA CTCAGGTCCT TTCCTTTCTG 1860
GGTCTTAAAC TTCCACACCC CCTTCCTTGA AGGTCCCTAT CCGCTCACCC CTGAGCTGAT 1920
GCTGAACACA GGCTGTACAG GAAGACCTAA GATTAATTTC TTCCCTTTGC TGGCTGCAAA 1980
GGACTCTCAT GGAAGGTGAG GCACTCAGAG TCCATGAGAC TGGCTGATCA TAAGGACTAC 2040
GACCAGCTGG GTAGAAGTCA GTTATGGAGG AAGCACAAGT TGGATTCAGC CAGGGGTGGT 2100
GGTTCACGCC TGTCATCCCA AACTTTGGGG GTCCGAGGCA GGACGATCGC TTGAGCCCGA 2160
AGTTTGAGAC CAGCCTAGGC AACATAGCAA ACCCTGTCTC TACAAAAAAA TTAGGCCAGG 2220
CACGGTGGCT CATGCCTGTA ATCCCAGCAC TTTGGGAGGC CGAGGCGGGT GGATCACTTG 2280
AGGTCAGGAG ATCGAGACGA CCCTGGCCAA CATGGTGAAA CCCCATCTCT ACTAAAAATC 2340
CAAAAATTAG CCGGGCGTGG TGGTGCAGCG CCTGTAGTCC CAGCTACTCA GGAGGCTGAG 2400
GCAGAGGAAT CGCTTGAACC CAGGAGGTGA CAATTGCAAT GAGCCGAGAT CATGCCACTG 2460
CACTCCAGAC TGGCGACAGA GTGAGACTCT GTCTCAAAAA AATTAAAAAA TTAAAAAATA 2520
AAAACTTAGC 2530