EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-44876 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr22:36770420-36771940 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2294358chr2236771256hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Stat6MA0520.1chr22:36770755-36770770CATTTCCTGGGAAAT+6.99
YY1MA0095.2chr22:36771237-36771249CAAGATGGCTGA+6.04
Number of super-enhancer constituents: 51             
IDCoordinateTissue/cell
SE_00116chr22:36744550-36773501Adipose_Nuclei
SE_00874chr22:36770572-36771835Adrenal_Gland
SE_01541chr22:36770573-36771936Aorta
SE_02243chr22:36770616-36771657Astrocytes
SE_02896chr22:36770545-36771535Bladder
SE_03974chr22:36770573-36771488Brain_Anterior_Caudate
SE_05865chr22:36762012-36771979Brain_Hippocampus_Middle
SE_09195chr22:36744556-36774047CD14
SE_10697chr22:36770597-36771935CD19_Primary
SE_11020chr22:36744527-36785336CD20
SE_11868chr22:36770468-36776664CD3
SE_13866chr22:36770540-36771953CD34_Primary_RO01536
SE_14476chr22:36770269-36771945CD4_Memory_Primary_7pool
SE_15971chr22:36771018-36771981CD4_Naive_Primary_7pool
SE_16932chr22:36770460-36771763CD4p_CD225int_CD127p_Tmem
SE_17339chr22:36756664-36780212CD4p_CD25-_CD45RAp_Naive
SE_17788chr22:36746596-36785463CD4p_CD25-_CD45ROp_Memory
SE_18286chr22:36744506-36778586CD4p_CD25-_Il17-_PMAstim_Th
SE_19119chr22:36756666-36778387CD4p_CD25-_Il17p_PMAstim_Th17
SE_20220chr22:36770449-36776653CD56
SE_21488chr22:36770561-36771640CD8_Naive_7pool
SE_21957chr22:36770386-36771932CD8_Naive_8pool
SE_22328chr22:36770356-36778565CD8_primiary
SE_23071chr22:36770524-36771855Colon_Crypt_1
SE_23740chr22:36770588-36771718Colon_Crypt_2
SE_24731chr22:36770657-36771414Colon_Crypt_3
SE_25782chr22:36756588-36771936Duodenum_Smooth_Muscle
SE_26521chr22:36758036-36775377Esophagus
SE_31378chr22:36770270-36773944Gastric
SE_35832chr22:36768543-36772008HMEC
SE_37948chr22:36745836-36771974HUVEC
SE_40597chr22:36770552-36771924Left_Ventricle
SE_41574chr22:36770634-36771714LNCaP
SE_42094chr22:36770414-36771946Lung
SE_44196chr22:36770588-36771633NHDF-Ad
SE_44762chr22:36770615-36771648NHLF
SE_45604chr22:36768504-36771979Osteoblasts
SE_46902chr22:36770713-36771642Ovary
SE_47169chr22:36744668-36771991Panc1
SE_48566chr22:36770454-36771921Right_Atrium
SE_50050chr22:36770402-36772120Sigmoid_Colon
SE_52340chr22:36770446-36771957Small_Intestine
SE_53283chr22:36767759-36772183Spleen
SE_54489chr22:36744394-36771971Stomach_Smooth_Muscle
SE_55183chr22:36770614-36771915Thymus
SE_58448chr22:36724049-36832686Ly1
SE_62244chr22:36719186-36785326Tonsil
SE_63497chr22:36770748-36771608HSMM
SE_64824chr22:36770423-36771831NHEK
SE_65307chr22:36770396-36773051Pancreatic_islets
SE_68689chr22:36770565-36771937H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr223677053636771368
Enhancer Sequence
CGGGCATGGC GGCACGCGCC TGTAATCCCG GCTACTCGGG AGGCTGAGGC AGGAGGATTG 60
CTTGAACCTG GGAGGCGGAG GTTGCAGTGA GCCAAGATTG TGACAGTACA CTCCAGCCTG 120
GGCGACAGAG TGAGACTCTG TTTCAAATAA TAATAATAAA TAAAAACAGA ACTGATTCTA 180
ATAACAATTA CGTCTCTCTC AATATTCCAT GAAAAATCTC ATCCCAAGTC CTTTGGCTAG 240
AAAAACATGC TGGCCACACA ACCAGAGGGC GCAGGCCGCG TTCCCAGCAT CCACCCCCAA 300
GGTGAGTGAC CTGGGAGTGG AATCCTGCAC TCCCACATTT CCTGGGAAAT GGGGCAAGGA 360
AACAAGCCTT CACGGGCCGT CTTGGCCTAT GCAGAGGCTG GGTCGTGGCC TAAGGAGGAG 420
AGGAAACGTT TCACCAGCCC CAGGTGACTC ACAGGGCCTT CACCAACCTG AATCACCCCT 480
GAACAAAGCT CTGCCTGCGT CTGGGCAACT GAACGAGGTC CCACCCCTGC TCCCTGGACT 540
TGCCACACCA TGTCTCTACT TTACAATCTC GAAGGCTGCC TCCTCCAGGA AGCCTTCTCA 600
GACTCCCCCC TGCCTTCTCC CTGGGTTTCC AGCATCGGTA TCTGGTGGGA GACCATCAGC 660
TCCCAGAAAC AAGGGCCTAT GTTTCTTTTC CCTCCATATT CCTAGCACCC AGCCAGTGCC 720
TTATACCTAG AATCAGTTCC TCCTAGTAGG AGTCACTGCT GAATGACTAT GAATCTGATG 780
GGTGGACAGA TGAAGGACGA AAGGAACCCA ATGGTTTCAA GATGGCTGAT GTCAAGAGCT 840
CACTAGGCAA CATGATGGCA GGTTGCCTGG CTAGCTGGTT CCCCAGAGGG CACTACTCAG 900
ACAGGCACAG CAGTGCCTGG ATTCACGCTG GGGCCAGGGT CTTTCCACCT GCTCTCCCTT 960
AGGACCAACC ACATTCATTT GAAAAATGGC CAGTGGGGTT AAAGGTGAAG TCAGTAGCCA 1020
AGGCATCAAT GCTGACCTGG CAACCCCGCT GTGGGTTGCC AACTGCTGTA CGGGAGATCC 1080
CATTCTGCTG CAGCCCAACG TTCTCTCTGC CCATTGAATG AATGCTCAGC CACTGGTGAG 1140
GGTGGAGGCC TCAAGGACCA GCCCAACCAC TCACCGCCAA GTGAGGAAAC ACAAGTCCTG 1200
GAGTGCAGGG CGTCTCCAAG GCCACAGAGT CAGGAGCTGG AGCACCCAAG TTTGAATCCC 1260
TGCACAGTCT CCCCATCTGC AAAATGAGGA TAAGTTCCTA CCTTATGGAA ACCAGGGAAG 1320
AATTAAATGA GATAATCCAT GTAAAAGCCC TAGCATGGCC AGGTGTAGGT GCAGTGGTGG 1380
CTCACGCCTA TAATCCCGGC ACATTGAGAG GCCAAGGTGG GAGGATCACC TGAGGCCAGA 1440
AGCTTGAGAC CAACCTGGAC AACACAGTGA GAGCCCATTT CCATTTTTTT AAATGTAAGT 1500
TAAAATTTTT TAAATAAAAG 1520