EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS043-22393 
Organism
Homo sapiens 
Tissue/cell
Fetal_heart 
Coordinate
chr2:47229340-47232620 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs17540621chr247229839hg19
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUN(var.2)MA0489.1chr2:47231406-47231420GTGAGTCACTTCCT-6.15
RFX1MA0509.2chr2:47229897-47229913TGTTGCCATGGTTACA-6.94
RFX1MA0509.2chr2:47229897-47229913TGTTGCCATGGTTACA+6.95
RFX2MA0600.2chr2:47229897-47229913TGTTGCCATGGTTACA+6.77
RFX2MA0600.2chr2:47229897-47229913TGTTGCCATGGTTACA-6.83
RFX5MA0510.2chr2:47229897-47229913TGTTGCCATGGTTACA-6.14
RFX5MA0510.2chr2:47229897-47229913TGTTGCCATGGTTACA+6.27
RORA(var.2)MA0072.1chr2:47230175-47230189CTGACCTAATTAAC-6.05
ZNF263MA0528.1chr2:47231802-47231823GAATGAGCAGGAGAAGGGAGG+6.27
Number of super-enhancer constituents: 19             
IDCoordinateTissue/cell
SE_00056chr2:47228729-47233257Adipose_Nuclei
SE_00864chr2:47228939-47232656Adrenal_Gland
SE_01547chr2:47229049-47237427Aorta
SE_03148chr2:47228934-47232779Brain_Angular_Gyrus
SE_03864chr2:47224295-47237133Brain_Anterior_Caudate
SE_04790chr2:47207331-47238050Brain_Cingulate_Gyrus
SE_05773chr2:47203345-47237435Brain_Hippocampus_Middle
SE_06717chr2:47224482-47237491Brain_Hippocampus_Middle_150
SE_07731chr2:47224149-47237360Brain_Inferior_Temporal_Lobe
SE_08824chr2:47229662-47231117Brain_Mid_Frontal_Lobe
SE_08824chr2:47231233-47231571Brain_Mid_Frontal_Lobe
SE_09141chr2:47226225-47233894CD14
SE_26122chr2:47229467-47230939Duodenum_Smooth_Muscle
SE_26616chr2:47229058-47231804Esophagus
SE_26616chr2:47231831-47232707Esophagus
SE_48626chr2:47229031-47231103Right_Atrium
SE_53323chr2:47229516-47230518Spleen
SE_54495chr2:47226285-47245145Stomach_Smooth_Muscle
SE_65882chr2:47229163-47232588Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr24723098247231623
Number: 2             
IDChromosomeStartEnd
GH02I047001chr24722903247231739
GH02I047004chr24723183247232707
Enhancer Sequence
CCCTAGGTTT AAATCCTGGG ATTAAATGCA TGGATTAAAC GGAGCAGTGC ATCCCCAGCG 60
CTGGGCAGCC TTGGGGTGGG TGTGGGGGTT ATGGCAGTGC ACACTAGGCA GGGAGAAACC 120
AGAGGAGAAC ATTCTGCCAT TATTCTAAGA ACAGTGAGGA AGAGACGGTG AGAAGATTTA 180
ATGTTCATGT ATTACTTTAA GGGTCACAAG TGCATTCACA TCTGTTACTG CATTTGATCT 240
AGAGGATTTT CTAATGAAAG AAAGCAGGAT TCTGAGGCCA CTTCAATGGT GGAAGGGAAA 300
GAGTGTGGCT GGGACTAGGT CAGAGCTACT CCCAGAGCAT GGGGGTACAC CATGTGGCCT 360
GAGGGCAGTG AGCCAGGGAG GAGGGAGCAG GACAGCTGGG GGTGCTGGGA AGGAACTGAT 420
GCTCCCATAG TGTCTGAGGC CCTGGCCTCA GAGGCTAGCC CTGGCCCCTG AGCTGCACAT 480
TAATTCTGTT CTGCTGTGGC TTACCCACCA GCCCCCATGC CTGCCTTTTC TCTGTCCCAT 540
TTCCCCCTAC CCCTCCCTGT TGCCATGGTT ACACACACAG GCACTGCCCA GCAACCACCA 600
GGAATATTTC ACTTCGGCCC TGCCCCAAAG CCATAGTAAC CACTCAGCCC ACTTCTGCTT 660
CTGGCTGGGG AATCACAGCC CTCTCTTGCA CAGGCCCCAG TTCGCACCAG TCCCTAGGAC 720
CCCCAGGGAG CCTTCCTGGC TGCCTGCCTA TTGAGGGCCT ATCACCAGCC TGAGGATTTG 780
TGCTGCTGCT GCTGCCGCTG CTGCTAGTAT GCTCCTCTCT TCTGTTCCTA TTCTTCTGAC 840
CTAATTAACG CCCGGTTCTG AAAATCCACC CCTCCCTCTG CCAGACACAA ATTCAGACAC 900
TGTTCTCTTA AAGGTCAAGG TCTAGGGTGG ACAGGGGGAG GTTTCCACTC CAGGCCCAGA 960
GTCTTTCTCT CCTGAGTGTC ACACCCTGCA GGTTGAGTCA AGTTCTGTGC GTGAGGCTGT 1020
GCCTGGGGCC AGGAGTCTAG CCATGAGCAA GAACTGGTGA ACCAGACGGG GGCATGTGAG 1080
CTGAGGCATG GGCTGGGTTG GGGGAGGACA GGAGAGGCCT GACCTCTCCT GGTGAGATGA 1140
GTTAGGGATG GTGCTGTAAG AGGGTGGTCC TGAATGGGGT TGTGAGGAGG TAGAAGGTGT 1200
CCAGGTTGAT AGAGGGAACT GCAGCATGAC CGAAGATGGG CCATGGTGAC TGTAGGGACC 1260
AGCAAGGGGT TCCATGTCAC TGGAGAGAAG CCCGCCAGTT AGGCTGCCCC AGAAAGGAGT 1320
TTAGATTTTA TCCTGATGGC CATAGTGATG GCTCGCAGCC CACTATCCCC TGAACAAGAT 1380
TGGTCTGCAC AGACAGGCAG GAGGGTCCCC AGACCCTGGA TGTGCCCAGC CAAGCTTCTT 1440
CCCACCCCTG CAGACTGCCT GGCTCCACCC GCTCCCATCA TAACCTCTTG CTTCCACCAG 1500
AATTCCAGGT CAGCCTCCAC TCGGGGATGT GCATCCTATA ATGCTGCTCC TTCCTGTTCT 1560
CCCCATGGGC AGGGCCTCTG TGCCCCCGTC CTCTCACACC CGAGCCACTC TTGCCTGTTG 1620
GAGGCCGCCC CTGTGGGTCC CCACCCTGGG TGGCCAGAGC TGGGGAGCTG CTGGAGGTGG 1680
TGGAGTGGGT CAGTACATCG CCGGGGACAG AACGAGGGCT GTATTCCTAG TTGGCTCAGG 1740
GGACTAGCTC CTGCCAACCC TCTCCCTAGA ATTTCTTCTC TCTTCCTGTT GGTGGCTGTG 1800
TGGGTGGACT TCACTGGGAA GGAGGGGGAT TTCTTGGCAC CTTCTTTCTC CACTCCTCTC 1860
CTTCAACCCT TTGGAGCTCC TGAGTGGCTC CTGTTCCACA GGCTGACTCC AGAGCTCAGC 1920
CTTGCCGGGA TTTCCGGGCA TCCCGGCACC CTCTCCTGGG CCATCTAAGT CCATGGGGGC 1980
ATGGGCAGCA CTCACCAACT GTGGCAACAG GGCAGCCATC AGAACCCCTG GCCACCAGTC 2040
TCTCAGTGAC TGAGCTGTCC CCCAGGGTGA GTCACTTCCT TGGGTCTTGG AGGTGTTTTG 2100
GCTTCCAGAG GCTTCTGGGA GGACTCCCTC CAGCCCTGCG CTGCAGGACA CACCCAGAGC 2160
CTGTGGTCTG GAGGCCTCAG GGGCTTGGGC TTCTGCCTCC AGCGCCTCAC CTGGAGGAGG 2220
GGAGAGCAGT CCTGCCCAAG GGAAGCTGTG AGGCCCACTT GCTGCATAGG AGGGATGGGG 2280
TAGCTCTGAT GAGGGAGATC TGGGTTTTTA GGGCTGGCAG CTCCTTTTTA TTCGGTTAGG 2340
AAGGCTGAGT CCTTGGTCTT GAGGTCCTGT GTATGGAAGC AGAGGAGGGC AAGTACTATT 2400
GTACAGAAGG AGGCTCAGAC AGAGGGAGGG AGATGCAGGA GAGAGCCCCA TTTGGCAGAG 2460
GGGAATGAGC AGGAGAAGGG AGGATGCTGG GGGCGGCCCC CAGCAGCATC TGCCCAGAAC 2520
ACAGCTCTGC CCAGCTCCCG CACAGCCCTT GGAGTGGGGG TGGATATGTT ACCATTTCTG 2580
GCCCCAGAGT GTCCTCTGCC TAAGTCCCTG CCCTGTGGCT GCTTGGAGGC CCCCATGACT 2640
CCTGCAGCTG AGGAGCTTCT CCCTTTCCAC CTTTTGCCCC CAGCCTGCGT GTTGCCCCCA 2700
GGGTATAGAG GTGGGCAGAG GGGTGGGACT ATCTGCACAT ACCAAAGAAC ACAAGAGTCC 2760
CACATCCTTG ATGGGGAGCT TCTGGCTTGG TGATGAGGAG CTCCCCTCTT GGAATTAGAC 2820
AGAATTTCCC GCTCATACAG CACCTTTCCC TCTCCTACCG CCACCCCCAG CAGCCATCTG 2880
GCAACTCTGT GAGCTACTGA AATCCTCGGC GCTGGACGCC AAGAGCAGAG TTCTTGAGTG 2940
TGGGGAAGCT CTCCCTGGGG AGGGACGGAG GAGAGTTTCC ATGGTTGGAA GGAGCCAGGA 3000
GAGGGTCCGG GCTGGACACA GAGAGGAAGG GAGGGGGGGG CTCTGGGAAT GTCGTTGTCA 3060
AAGCTACTTG AGAGGCTGAA GAGGAAGAGA AGAGGGCACT GGGGGCCACA GCCCAACCTC 3120
CCCACCAAGA GTCAAGCAGC AGAGCCACCT ACCCAATCCA GGCACTTTCA CATCTTAGCC 3180
AAAACTCTTG CTGTAATTGT GAGAATTGCA AACACACCAG GGACTGTTCC ATAAAACGAC 3240
TGGCCTGTGC TCCTCAAAAA TGCCAGTGTC ATGAGAGAGA 3280