EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS177-09192 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH_RA 
Coordinate
chr17:38487840-38489100 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr17:38488179-38488200TGGGGAGGATGAGAGGGAGGG+6.81
ZfxMA0146.2chr17:38488510-38488524GGAGCCGGGGCCTG+6.13
Number of super-enhancer constituents: 48             
IDCoordinateTissue/cell
SE_00190chr17:38485716-38489696Adipose_Nuclei
SE_00975chr17:38486095-38489398Adrenal_Gland
SE_01678chr17:38485949-38489535Aorta
SE_03802chr17:38488733-38489115Brain_Angular_Gyrus
SE_04480chr17:38486156-38489321Brain_Anterior_Caudate
SE_06212chr17:38486078-38489557Brain_Hippocampus_Middle
SE_08413chr17:38486057-38489326Brain_Inferior_Temporal_Lobe
SE_09193chr17:38472951-38489514CD14
SE_10906chr17:38473531-38488563CD20
SE_14465chr17:38485818-38488661CD4_Memory_Primary_7pool
SE_17354chr17:38485821-38488579CD4p_CD25-_CD45RAp_Naive
SE_17774chr17:38485522-38489304CD4p_CD25-_CD45ROp_Memory
SE_18539chr17:38485708-38488289CD4p_CD25-_Il17-_PMAstim_Th
SE_19121chr17:38488379-38489288CD4p_CD25-_Il17p_PMAstim_Th17
SE_23986chr17:38488475-38488782Colon_Crypt_2
SE_25047chr17:38488152-38489001Colon_Crypt_3
SE_25879chr17:38487989-38489640Duodenum_Smooth_Muscle
SE_26766chr17:38486155-38489390Esophagus
SE_27821chr17:38487816-38488591Fetal_Intestine
SE_28846chr17:38487614-38488992Fetal_Intestine_Large
SE_29564chr17:38486074-38489453Fetal_Muscle
SE_31511chr17:38486156-38492308Gastric
SE_33936chr17:38486056-38489537HCC1954
SE_34507chr17:38488068-38488790HCT-116
SE_35094chr17:38487643-38489431HeLa
SE_37177chr17:38488031-38489535HSMMtube
SE_38107chr17:38487668-38489447HUVEC
SE_40737chr17:38486164-38489427Left_Ventricle
SE_41732chr17:38486065-38489228LNCaP
SE_42126chr17:38485934-38489462Lung
SE_44282chr17:38487637-38489396NHDF-Ad
SE_44952chr17:38488081-38489103NHLF
SE_45871chr17:38487600-38489430Osteoblasts
SE_46732chr17:38487581-38489094Ovary
SE_47329chr17:38486053-38489659Panc1
SE_47571chr17:38486235-38489223Pancreas
SE_48093chr17:38485990-38489532Psoas_Muscle
SE_48589chr17:38486024-38489418Right_Atrium
SE_49515chr17:38487999-38489162Right_Ventricle
SE_50100chr17:38486010-38489401Sigmoid_Colon
SE_51122chr17:38485628-38492123Skeletal_Muscle
SE_52419chr17:38486106-38489309Small_Intestine
SE_53319chr17:38485880-38492398Spleen
SE_54720chr17:38485808-38489706Stomach_Smooth_Muscle
SE_59903chr17:38465110-38509835Ly4
SE_61531chr17:38458893-38531888Toledo
SE_62713chr17:38462659-38504649Tonsil
SE_65331chr17:38486006-38489283Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr173848801538488253
Number: 1             
IDChromosomeStartEnd
GH17I040329chr173848590138489831
Enhancer Sequence
GTTGTGTTTG AAGTTGGGGG TGGCAGAGGG GGAGATGAAA CCATGCTGTT CTGGCCTGCA 60
GTGGCCCTCG CACCCCTCTT CTGTGCTCTG CTGTTGGGGC CTTATAAATA GCTCCAAGGA 120
CTGGACACAC AGGTTGGAGG TGGGTAAACA AACCTCTTGA CATTTGATGG AAATGGCAGC 180
TCTACCTAGA GTGAGAGCAG CACACCACCT ACGCCCCACC CCCACTCAGT GCCTCTGAGG 240
GAAAGGGCTT GAAGGAGCAG ACCGAGGAAG GCTGGCTGGA ACCCCACCTC TCCCCCTGCC 300
AGCTCCACCC CCGGCCATGC TAGGATGTGC TTCCCTTTGT GGGGAGGATG AGAGGGAGGG 360
GCCCACGGTC TAGCTGGGTG GATAGGGTGA GTGTCCCAGG AGGGGACACT TGGCCTGGAC 420
TCTGGCCTCG GACGCATGCA TGGTCTTGGC AGGGCCTGTG TTTTCCTTGC CTCCACCCTC 480
TGCCATGGAG GTCACTTGTT GGCTGGGCAG GGGTCTCAGT ACCCTTCGCC GGCTGGCCGA 540
GCCAGGTAGT GGGAGGTGGC GGCAGCTCTG GCCAGCTGGC AGAGTCCAGG GCTGGGGCCT 600
GCCAGGCCGC TTACAGTAAC TCTGGCCCCC AGGGCCCAGC TGGGCGCCAG GCCAGGGCTG 660
GGGGGAGGAG GGAGCCGGGG CCTGGCCTGG GACGGGAGAG GGTGGAAGCA GCAGAATGGG 720
CCATGGGCTG CTGGCTGGCC GGCTGGTCAG CTGCTGACCT GGGAAACGTG TCCCCACCTC 780
TCCTGGCCAG CAGGGACTGC ACACCTTGCC CTGTGCACCC ACCACCCCTC TCACGGCTGC 840
TGGCAAGCTG CCTGGCACCA CTGCCCTATG TGCCTGGCTG GGCTGGGTCA GTGCCCCCTT 900
CTCAGTGTGG GGGCAGCGCT CTCTCCCCGG AGCCAGGGAG TCTCTTTGTC CCTGGGGCAG 960
GCCCTGGCTG GGCGCCTCAC TGCCCGCACT GGCTGGGTGC CCACCACCAC CACTGCTTCC 1020
TGGATCGCCT CCTCTGGCTT AGCTGTGGCC CCCTCCCTCC CAGGCTCCAC CAGCCACCAG 1080
GAGCAGGGAC TCTATGTCTG TGTTTCTTTG TGTTCCCCGC CCTTTATGCC CTGGGGCCAG 1140
GGGGCAGGCA GGTGCTGCCT CAGTTTCTCC TGCCACCCCT TATCAAACCT TCATCTTCTG 1200
TTTCTGCTGT CTCTTCTCTC CACCTCATAT AGGAGTATGG GATGGATGGA GTCTGGGGAC 1260