EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS048-00524 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr1:21655170-21658120 
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
GCTTGAACCT GGGAGATGGA GGTTGCAGTG AGTTGAGGTC ACTCCACTGT ACTCCAGCCT 60
GAGCAACAAG AGCGAACCTC CATCTCGAAA AAAAAAAAAA AAAAAAAAAG AATCTCTGTG 120
TGGAAGTCTG CAAAAGCAAC CACGTTGGGT ATTAGGAGGA ACACAGGCCT CGGCTGCTGA 180
GGGTCTGCTT TCTAATCCCA GCTCTGCCAC CACAAGCTTT GGGCAAGGTA CCGCCTCTCT 240
GAGCCTCAGT TTCCTTATCC AATTGATCTA AAGGTGGAAT GGACATGCTG GCTGTTCATC 300
ATGACTGCTG CGAATCTCTC TCTAGACTCC CACCTCCCTT TGCATCCATT CCCCCTACCA 360
GGCGATGTTC TGATGGCTGA AGTGACCAAA TAAAATGCCC AGGATAGTGT TGGACCCAGA 420
GAAGACATGT AATAAATTAG ATTTCTAGCA TATTCTATGG TCCACCAGCA TCAGAATCAG 480
GCATTCTGCT GGAAATGTAG GTTCCTGGAC CCTCCCCCCG ACACTTACTG AGTTAGAACC 540
TCTAGGATGA GGGCAATGAA ACTTGCATTT GTAACCAGCA TTCCTGATGA TTCTCATGCA 600
CATGTCCGTT GAGAAGCACT GAAATCAATG CAACCTTATG CTTGCTACCG CCGACTTGCA 660
ATTCCTGGGT GTCCTGATTA CCAGCACAGA GGTGAGACTC ACCAGAAAGG GGCGTGGCCT 720
TCATAACCTG GTATTCTTCC TGATGGCTTA AAAACACGAG TACAGGCCTT GCAGTTAGAT 780
TGAGGTGCAA ATTCCAGTCC CTCTACTTAC TGGCTTAGCT GTGTGACCTT GGACACATGG 840
CTCAACCTCT GTGAGTCACC TTTCTCATGC TTAAAACGGC AGTAAATTAC CTCTACCTGC 900
CAGGGTTGTT GCAATGATCT GAGGAGGTGC CTTATGCAAA GCACAGTTCA TGTGCTCGGG 960
GCAAACAGTG GAAAAACAAA CCAGGAAATG CTTCTCTGTC TGTCTGTGCC TCCTACCTGC 1020
CACAGGAGAA CTGAGGGTAG AATCTGTGTA CCCTTCTCAG CACACCACAA ATCCTAGTCA 1080
CTTAGAGAGA CACAGACTGC CTACAAGGCT AGTCAACTCC CAACCACCTT TGCAGAAGGG 1140
GGAGAGAGTG GGAGTTTGTG AAGAGCAAAA GCAGGAATTG GATGGGAAAA TGGTCTAGGG 1200
CTCACGTGGA GTGACCCAGG ACCCAGAGTC TCACCTCCCA AGGCTAGGCC TTGTAGGGCA 1260
GCAGGGCCAA GCATGCTGCA GGAAAGAACA CAGAGTCTGG AGCCAGACTG TTCAGGTTTA 1320
AATTTTGGCT CTGCTACTAC TAGCTTTGCC TGGCTGGCAA ACTCCTACCC ATCCTTCAAG 1380
ACCCAACTCA AACATCACCT CCCTGGACCA AGTTACTGGG CCTTTAAAGG CTCCTGCCCA 1440
CATACTCACT AAATACTTTT TTTTTTTTTT TTTTTTTTTT GAGACAGAGT CTCCCAGGTC 1500
CTATTCCTCT GGGCCTTTAA AGGCTCCTGC CCACATACTC GCCAAATACT TTTTTTTTTT 1560
TTTTTTTTTT TTTTTTGAGA CAGAGTCTCC CTCTGCCACC CAGGCTGGAG TGCAGTGGCA 1620
TGATCTCCAC TCACTGCAAC CTCTGCCTCC CGGGTTCAAG TGATTCTCAG CCTCCTGAGT 1680
AGCTGGGACC AAAGGCACGT GCCACCATGC CCAGCTAATT GTTTCGTATT TTTTGTAGAG 1740
ATGGGGTTTT GTCATGTTGC CCAGACTGGT CTCGAACTCC TGGCCTCAAG TGACCCACCC 1800
ATCGCAGCCT CCCAAAGTTC TGGGATTACA GGTGTGAGCT ACCGCCCCTA GCTGACCTCA 1860
CCAAATACTA TTCAGCAATT TACCTGCTAA TTTATCTATC TCTCCCACAG GCCTGGGAGC 1920
TCCTGGAAGG CACAGACACT GCCATGCCTG GCACAGGAAA CGTACTCAGC AAATGTTGCT 1980
TCAGTTTGAA TGCCAACTTT TTCAGCCTTC TGAGTTTCCT TTCTCTCCCC ATTAAATGCT 2040
TCCTAGGCTA ATCCTTCTTC CTCCCCCTGA CTCAGGTCCT TTCCTTTCTG GGTCTTAAAC 2100
TTCCACACCC CCTTCCTTGA AGGTCCCTAT CCGCTCACCC CTGAGCTGAT GCTGAACACA 2160
GGCTGTACAG GAAGACCTAA GATTAATTTC TTCCCTTTGC TGGCTGCAAA GGACTCTCAT 2220
GGAAGGTGAG GCACTCAGAG TCCATGAGAC TGGCTGATCA TAAGGACTAC GACCAGCTGG 2280
GTAGAAGTCA GTTATGGAGG AAGCACAAGT TGGATTCAGC CAGGGGTGGT GGTTCACGCC 2340
TGTCATCCCA AACTTTGGGG GTCCGAGGCA GGACGATCGC TTGAGCCCGA AGTTTGAGAC 2400
CAGCCTAGGC AACATAGCAA ACCCTGTCTC TACAAAAAAA TTAGGCCAGG CACGGTGGCT 2460
CATGCCTGTA ATCCCAGCAC TTTGGGAGGC CGAGGCGGGT GGATCACTTG AGGTCAGGAG 2520
ATCGAGACGA CCCTGGCCAA CATGGTGAAA CCCCATCTCT ACTAAAAATC CAAAAATTAG 2580
CCGGGCGTGG TGGTGCAGCG CCTGTAGTCC CAGCTACTCA GGAGGCTGAG GCAGAGGAAT 2640
CGCTTGAACC CAGGAGGTGA CAATTGCAAT GAGCCGAGAT CATGCCACTG CACTCCAGAC 2700
TGGCGACAGA GTGAGACTCT GTCTCAAAAA AATTAAAAAA TTAAAAAATA AAAACTTAGC 2760
CGGGTATGGT GGTGCACGCT TGTAGTCTCA GTTACTCGAG AGGCTGAGGT GGGAGGATCG 2820
CTTGAGTCTG GGAGGTTGAG GTTGCAGTGA GCCATGATGC ACGATGGTGC CATTGCATTC 2880
CAGCCAGGGT GACAGGCAGA GTGAGACTTC GCTAAAAAAA AGAAAAAAAA AAGCATAGAC 2940
TCTGTAGCCA 2950